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Equipo de orina", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas para la licitaci\u00f3n del analizador automatizado del sedimento de la orina. Hemos notado en el punto donde se detallan los reactivos, que se solicita que \"Los reactivos tiras de orina deber\u00e1n ser suministrados en formato de cassette de an\u00e1lisis sellado, de tal forma de evitar posible contaminaci\u00f3n de los reactivos o el deterioro de las almohadillas reactivas por humedad\". Si bien entendemos la preocupaci\u00f3n por la integridad de los reactivos, consideramos que esta especificaci\u00f3n, que exige un formato de cassette sellado, resulta ser excesivamente dirigida y podr\u00eda limitar la libre competencia. En la pr\u00e1ctica, las tiras reactivas de orina que vienen en formatos de envase m\u00e1s comunes (como botes con desecante) son igualmente funcionales y eficaces para evitar la contaminaci\u00f3n y el deterioro por humedad de las almohadillas reactivas, siempre y cuando se sigan las instrucciones de almacenamiento y uso del fabricante. Solicitamos amablemente que se reconsidere esta especificaci\u00f3n, permitiendo la oferta de tiras reactivas que garanticen la estabilidad y protecci\u00f3n de las almohadillas reactivas, independientemente de si vienen en formato de cassette sellado o en otros envases igualmente v\u00e1lidos y funcionales, lo cual fomentar\u00eda una mayor participaci\u00f3n y opciones de equipos en la licitaci\u00f3n.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:57-04:00"}, {"id": "ce68ba2cf379ef0f946e29584dd4aae2-1", "date": "2025-06-09T08:14:21-04:00", "title": "PLAZO DE ENTREGA", "description": "Se solicita a la convocante especificar el plazo de entrega de los insumos que no requieren equipos en comodato. En el apartado \u201cPlan de Entrega\u201d del Pliego, \u00fanicamente se detallan el \u201cProcedimiento de Entrega de \u00d3rdenes de Compras\u201d y el \u201cCronograma de Entrega\u201d correspondiente a los reactivos con equipo en comodato. Sin embargo, no se especifica el plazo de entrega para aquellos insumos que no necesitan equipos. Por favor, aclarar esta informaci\u00f3n para un adecuado cumplimiento de las bases", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:45:35-04:00"}, {"id": "9d6f8ada12e2cf72e47f3919c54ac3cb-1", "date": "2025-11-10T09:08:59-04:00", "title": "PLAN DE ENTREGA DE LOS BIENES", "description": "En el apartado de PLAN DE ENTREGA DE LOS BIENES, en el punto SALDO DE LA CANTIDAD M\u00cdNIMA, donde menciona: \u201cConforme a la necesidad del servicio. El proveedor deber\u00e1 entregar el bien solicitado dentro de los 10 (diez) d\u00edas calendario de haber retirado la Orden de Compra.\u201d Se solicita atentamente a la entidad convocante extender el plazo de entrega a 45 d\u00edas calendario, teniendo en cuenta que la modalidad de suministro ser\u00e1 conforme a las necesidades del servicio, por lo que no es posible conocer de antemano la cantidad exacta que se requerir\u00e1 ni planificar una producci\u00f3n espec\u00edfica con antelaci\u00f3n. Este plazo ampliado resulta necesario para contemplar los tiempos habituales de fabricaci\u00f3n, log\u00edstica internacional, procesos de importaci\u00f3n y tr\u00e1mites aduaneros, los cuales pueden superar f\u00e1cilmente los 30 d\u00edas, aun en condiciones operativas normales. Mantener el plazo actual podr\u00eda limitar injustificadamente la participaci\u00f3n de oferentes que no cuenten con stock inmediato, favoreciendo \u00fanicamente a quienes disponen de inventario local, lo cual introduce un sesgo competitivo contrario a los principios de igualdad, libre concurrencia y transparencia que deben regir los procesos de contrataci\u00f3n p\u00fablica. Por todo lo expuesto, se solicita que dicho requerimiento quede redactado de la siguiente manera: \u201cConforme a la necesidad del servicio. El proveedor deber\u00e1 entregar el bien solicitado dentro de los 45 (cuarenta y cinco) d\u00edas calendario de haber retirado la Orden de Compra.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:07:41-04:00"}, {"id": "7d0b97f37c5215c07155e07356be67b9-1", "date": "2025-11-10T09:06:04-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 49, \u00edtem 1: (Test R\u00e1pido para Influenza), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita amablemente a la entidad convocante considerar la admisi\u00f3n de pruebas r\u00e1pidas para detecci\u00f3n de Influenza A y B con una sensibilidad m\u00ednima del 87% y una especificidad m\u00ednima del 94%, par\u00e1metros que se encuentran dentro de los rangos internacionalmente aceptados para test de tamizaje o diagn\u00f3stico r\u00e1pido en entornos cl\u00ednicos y comunitarios. Tanto la sensibilidad del 87% como la especificidad del 94% garantizan una adecuada confiabilidad diagn\u00f3stica, especialmente para pruebas utilizadas en el primer nivel de atenci\u00f3n o en situaciones donde se requiere una detecci\u00f3n r\u00e1pida, accesible y operativamente eficiente. Estos valores son comunes y cl\u00ednicamente aceptables para pruebas de inmunoensayo cualitativas, seg\u00fan lo reportado en literatura cient\u00edfica y recomendaciones de organismos como la OMS. Adem\u00e1s, esta modificaci\u00f3n no compromete el objetivo sanitario del proceso ni la utilidad cl\u00ednica del test, pero s\u00ed ampl\u00eda la posibilidad de participaci\u00f3n de m\u00e1s oferentes, fomentando una mayor competencia en la adquisici\u00f3n p\u00fablica, sin perjuicio de la calidad del reactivo. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 87% de sensibilidad y 94% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:35:21-04:00"}, {"id": "c2b29fea114b9a2814746a5de3e068ca-1", "date": "2025-11-10T09:07:59-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita respetuosamente a la entidad convocante aceptar pruebas r\u00e1pidas para la detecci\u00f3n de Dengue ant\u00edgeno NS1 y anticuerpos IgG/IgM que presenten una sensibilidad m\u00ednima del 95% y una especificidad m\u00ednima del 96%. Estos valores se encuentran dentro de los rangos com\u00fanmente aceptados a nivel internacional para pruebas de tamizaje serol\u00f3gico y de ant\u00edgeno, utilizadas en contextos cl\u00ednicos y comunitarios. Tanto la sensibilidad del 95% como la especificidad del 96% aseguran una confiabilidad diagn\u00f3stica adecuada, especialmente en situaciones donde se requiere una detecci\u00f3n r\u00e1pida y efectiva, como en el primer nivel de atenci\u00f3n y en zonas con alta circulaci\u00f3n viral. Estos valores son frecuentes y considerados cl\u00ednicamente v\u00e1lidos en pruebas r\u00e1pidas de inmunoensayo cualitativas, seg\u00fan la literatura cient\u00edfica y las recomendaciones de organismos internacionales como la Organizaci\u00f3n Mundial de la Salud (OMS) y la Organizaci\u00f3n Panamericana de la Salud (OPS). Esta modificaci\u00f3n no compromete la eficacia cl\u00ednica del test requerido, pero favorece a una mayor participaci\u00f3n de oferentes, lo que promueve un proceso de adquisici\u00f3n m\u00e1s competitivo y equitativo, sin afectar la calidad del reactivo ni su desempe\u00f1o diagn\u00f3stico. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 95% de sensibilidad y 96% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:32:56-04:00"}, {"id": "111217049fe3131a72bfb47f26545414-1", "date": "2025-06-10T15:50:18-04:00", "title": "Lote N\u00ba 12", "description": "Solicitamos encarecidamente a la convocante modificar el precio referencial a por lo menos a  3.000 Gs por determinaci\u00f3n, favor verificar los precios ofertados en licitaciones anteriores con vuestra instituci\u00f3n correspondiente al a\u00f1o 2024, para que no sea declarado desierto por la discrepancia que pudiera existir con el precio actual del mercado.", "answer": "La determinaci\u00f3n del precio referencial se realiz\u00f3 con la aplicaci\u00f3n de las metodolog\u00edas contempladas en la Resoluci\u00f3n DNCP N\u00b0 454/2024. El precio referencial no es restrictivo ni condicionante.", "dateAnswered": "2025-11-11T11:45:41-04:00"}, {"id": "fb09de2a7ea97f238af8dec9e0a1c48d-1", "date": "2025-06-11T14:38:15-04:00", "title": "LOTE 1; ITEM 1 Equipo de Hemograma", "description": "Hemos notado que en el punto 1.c. se solicita una \"Medici\u00f3n m\u00ednima: 45 par\u00e1metros hematol\u00f3gicos\", mientras que en el punto 3. se indica \"Con capacidad como m\u00ednimo 24 par\u00e1metros hematol\u00f3gicos\". Agradecer\u00edamos que pudieran aclarar cu\u00e1l es la cantidad m\u00ednima de par\u00e1metros hematol\u00f3gicos requeridos para el equipo, si 45 o 24. Aclarar este punto nos permitir\u00e1 presentar una oferta que se ajuste con mayor precisi\u00f3n a sus necesidades.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:28-04:00"}, {"id": "9d22b8adca0806e3ccacbf68fa3de064-1", "date": "2025-11-10T09:03:37-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 47, \u00edtem 1: (Test R\u00e1pido para CHAGAS), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ANTICUERPOS IgG de CHAGAS en suero. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita a la convocante admitir una sensibilidad del 94% y una especificidad del 96% como m\u00ednimo ya que esta sensibilidad y especificidad siguen siendo altamente efectivas para pruebas de tamizaje, y son las m\u00e1s comunes para estos tipos de pruebas. Adem\u00e1s, de esta manera tambi\u00e9n permitir\u00eda una mayor participaci\u00f3n de oferentes. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ANTICUERPOS IgG de CHAGAS en suero. Con 94% de sensibilidad y 96% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:32:14-04:00"}, {"id": "0fb6c4d8bd800134bf4cb7874532aa5d-1", "date": "2025-11-10T09:08:11-04:00", "title": "PLAN DE ENTREGA DE LOS BIENES", "description": "En el apartado de PLAN DE ENTREGA DE LOS BIENES, en el punto CANTIDADES M\u00cdNIMAS, donde menciona: \u201cENTREGA DE LA CANTIDAD M\u00cdNIMA (20%): Una vez emitida la orden de compra por el administrador del contrato; el oferente tendr\u00e1 un plazo de hasta 5 (cinco) d\u00edas calendario para la entrega de los productos adjudicados a partir de la recepci\u00f3n de la Orden de Compra. En caso de requerir ajustar (cantidad de determinaciones por frascos/presentaci\u00f3n, las determinaciones podr\u00e1n ajustarse) las determinaciones a la o hasta las determinaciones contenidas en la presentaci\u00f3n.\u201d Se solicita amablemente a la convocante extender el plazo de entrega a 45 d\u00edas calendario, considerando los tiempos necesarios para la fabricaci\u00f3n, log\u00edstica de env\u00edo y tr\u00e1mites aduaneros, que pueden superar f\u00e1cilmente un mes. No ampliar este plazo resulta claramente discriminatorio y limita injustificadamente la participaci\u00f3n de oferentes capaces de cumplir con el suministro. Al mantener el plazo actual, se favorece de manera evidente a aquellos que ya disponen del producto en stock, demostrando un sesgo hacia ciertos oferentes. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cENTREGA DE LA CANTIDAD M\u00cdNIMA (20%): Una vez emitida la orden de compra por el administrador del contrato; el oferente tendr\u00e1 un plazo de hasta 45 (cuarenta y cinco) d\u00edas calendario para la entrega de los productos adjudicados a partir de la recepci\u00f3n de la Orden de Compra. En caso de requerir ajustar (cantidad de determinaciones por frascos/presentaci\u00f3n, las determinaciones podr\u00e1n ajustarse) las determinaciones a la o hasta las determinaciones contenidas en la presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:22:24-04:00"}, {"id": "30c5ceff5fd7b5d54c30bf33c95c3e88-1", "date": "2025-06-18T08:09:05-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 47, \u00edtem 1: (Test R\u00e1pido para CHAGAS), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ANTICUERPOS IgG de CHAGAS en suero. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita a la convocante admitir una sensibilidad del 94% y una especificidad del 96% como m\u00ednimo ya que esta sensibilidad y especificidad siguen siendo altamente efectivas para pruebas de tamizaje, y son las m\u00e1s comunes para estos tipos de pruebas. Adem\u00e1s, de esta manera tambi\u00e9n permitir\u00eda una mayor participaci\u00f3n de oferentes. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ANTICUERPOS IgG de CHAGAS en suero. Con 94% de sensibilidad y 96% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:59-04:00"}, {"id": "80bd816684361e6b2555753e4650be0b-1", "date": "2025-06-11T14:38:39-04:00", "title": "LOTE 14 TEST PARA MONONUCLOSIS", "description": "Con el objetivo de facilitar la participaci\u00f3n de un mayor n\u00famero de proveedores y ofrecer una mayor flexibilidad en las presentaciones de los reactivos, solicitamos amablemente que se acepte un formato de presentaci\u00f3n de hasta un m\u00e1ximo de 100 determinaciones por kit o envase en lugar de limitar a un m\u00e1ximo de 40 determinaciones.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:09-04:00"}, {"id": "12a3c19c79b73041e29f9cec11799c4b-1", "date": "2025-11-10T09:06:51-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita cordialmente a la entidad convocante aceptar presentaciones que contengan un m\u00ednimo de 20 determinaciones por caja, siempre que se garantice el cumplimiento del n\u00famero total de pruebas requerido en el pliego. Esta modificaci\u00f3n no afecta la utilidad ni la eficacia del test en su aplicaci\u00f3n diagn\u00f3stica. Asimismo, esta medida contribuir\u00eda a ampliar la participaci\u00f3n de oferentes, promoviendo un proceso de adquisici\u00f3n m\u00e1s competitivo, inclusivo y transparente. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:36:29-04:00"}, {"id": "d7c85c5ba8267e47269ad2091400eb86-1", "date": "2025-06-11T14:38:38-04:00", "title": "Lote 1 Equipo de Orina", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas para la licitaci\u00f3n de un Analizador automatizado del sedimento de la orina. Hemos observado una discrepancia en la cantidad m\u00ednima de par\u00e1metros cuantitativos solicitados para el analizador de sedimento. En el punto 3., se menciona que el equipo debe tener \"capacidad de detecci\u00f3n de eritrocitos, leucocitos, c\u00e9lulas epiteliales escamosas, c\u00e9lulas epiteliales no escamosas, bacterias, cilindros, cristales, levaduras y espermatozoide, como m\u00ednimo\", lo que implica 10 elementos m\u00ednimos. Sin embargo, en el mismo punto, m\u00e1s adelante se solicita \"reporte de por lo menos de 15 par\u00e1metros cuantitativos\". Agradecer\u00edamos que pudieran aclarar cu\u00e1l es el n\u00famero exacto de par\u00e1metros cuantitativos m\u00ednimos requeridos para el reporte del analizador de sedimento (si 10 o 15). Esta clarificaci\u00f3n es fundamental para poder presentar una oferta que se ajuste con precisi\u00f3n a sus requisitos. Sugerimos solicitar un m\u00ednimo de 10 par\u00e1metro, para fomentar una mayor participaci\u00f3n y ofrecer flexibilidad a los oferentes", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:04-04:00"}, {"id": "9542d3bab446f14ead76f2210b473d3a-1", "date": "2025-06-18T08:11:32-04:00", "title": "PLAN DE ENTREGA DE LOS BIENES", "description": "En el apartado de PLAN DE ENTREGA DE LOS BIENES, en el punto CANTIDADES M\u00cdNIMAS, donde menciona: \u201cENTREGA DE LA CANTIDAD M\u00cdNIMA (20%): Una vez emitida la orden de compra por el administrador del contrato; el oferente tendr\u00e1 un plazo de hasta 5 (cinco) d\u00edas calendario para la entrega de los productos adjudicados a partir de la recepci\u00f3n de la Orden de Compra. En caso de requerir ajustar (cantidad de determinaciones por frascos/presentaci\u00f3n, las determinaciones podr\u00e1n ajustarse) las determinaciones a la o hasta las determinaciones contenidas en la presentaci\u00f3n.\u201d Se solicita amablemente a la convocante extender el plazo de entrega a 45 d\u00edas calendario, considerando los tiempos necesarios para la fabricaci\u00f3n, log\u00edstica de env\u00edo y tr\u00e1mites aduaneros, que pueden superar f\u00e1cilmente un mes. No ampliar este plazo resulta\n\nclaramente discriminatorio y limita injustificadamente la participaci\u00f3n de oferentes capaces de cumplir con el suministro. Al mantener el plazo actual, se favorece de manera evidente a aquellos que ya disponen del producto en stock, demostrando un sesgo hacia ciertos oferentes. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cENTREGA DE LA CANTIDAD M\u00cdNIMA (20%): Una vez emitida la orden de compra por el administrador del contrato; el oferente tendr\u00e1 un plazo de hasta 45 (cuarenta y cinco) d\u00edas calendario para la entrega de los productos adjudicados a partir de la recepci\u00f3n de la Orden de Compra. En caso de requerir ajustar (cantidad de determinaciones por frascos/presentaci\u00f3n, las determinaciones podr\u00e1n ajustarse) las determinaciones a la o hasta las determinaciones contenidas en la presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:51:55-04:00"}, {"id": "ec2b1aea40bb02ea01336c25afb16262-1", "date": "2025-11-10T09:04:45-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 48, \u00edtem 1: (Test R\u00e1pido para Rotavirus), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99 % de sensibilidad y 99 % de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita amablemente a la convocante admitir una presentaci\u00f3n de 20 determinaciones por caja como m\u00ednimo, ya que esto no afecta la finalidad de uso del test ni compromete su efectividad. Adem\u00e1s, se respetar\u00eda el n\u00famero total de pruebas solicitadas, garantizando el cumplimiento de los requerimientos sin alterar el objetivo del proceso. Esta modificaci\u00f3n tambi\u00e9n favorecer\u00eda la participaci\u00f3n de un mayor n\u00famero de oferentes, promoviendo un proceso m\u00e1s justo y transparente para todos. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99 % de sensibilidad y 99 % de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:34:10-04:00"}, {"id": "6a42775e8189e455c5767f4807f78333-1", "date": "2025-11-10T08:58:46-04:00", "title": "Lote 12 Factor Reumatoide", "description": "\u00bf Podemos presentar certificado de libre venta de origen en vez de certificado de calidad ?", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:24:22-04:00"}, {"id": "dc3404e1fccf2ce7ebe1b22f0fdc35f8-1", "date": "2025-06-10T16:32:43-04:00", "title": "Lote N\u00ba 25", "description": "Solicitamos encarecidamente a la convocante modificar el precio referencial a por lo menos a  1.000.000 Gs x unidad, favor verificar los precios ofertados en licitaciones anteriores con vuestra instituci\u00f3n correspondiente al a\u00f1o 2024, para que no sea declarado desierto por la discrepancia que pudiera existir con el precio actual del mercado.", "answer": "La determinaci\u00f3n del precio referencial se realiz\u00f3 con la aplicaci\u00f3n de las metodolog\u00edas contempladas en la Resoluci\u00f3n DNCP N\u00b0 454/2024. El precio referencial no es restrictivo ni condicionante.", "dateAnswered": "2025-11-11T11:45:48-04:00"}, {"id": "dbb0122e949909001140b8c860a902f4-1", "date": "2025-11-10T09:02:52-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 20, \u00edtem 1: (TEST PARA SANGRE OCULTA), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. M\u00e9todo inmunol\u00f3gico para la detecci\u00f3n de hemoglobina en las heces frescas. Presentaci\u00f3n de entrega: Capacidad de realizar entre 25 y 50 determinaciones por presentaci\u00f3n.\u201d Se solicita amablemente a la convocante admitir una presentaci\u00f3n de 20 determinaciones por caja como m\u00ednimo, ya que esto no afecta la finalidad de uso del test ni compromete su efectividad. Adem\u00e1s, se respetar\u00eda el n\u00famero total de pruebas solicitadas, garantizando el cumplimiento de los requerimientos sin alterar el objetivo del proceso. Esta modificaci\u00f3n tambi\u00e9n favorecer\u00eda la participaci\u00f3n de un mayor n\u00famero de oferentes, promoviendo un proceso m\u00e1s justo y transparente para todos. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. M\u00e9todo inmunol\u00f3gico para la detecci\u00f3n de hemoglobina en las heces frescas. Presentaci\u00f3n de entrega: Capacidad de realizar entre 20 y 50 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:30:05-04:00"}, {"id": "4b351f5070b4af8bebab683072019257-1", "date": "2025-06-13T14:17:42-04:00", "title": "Lote 1 \u2013 Tiras de Orina", "description": "Solicitamos a la convocante considerar la separaci\u00f3n del \u00cdtem 83 del Lote 1, correspondiente a Tiras Reactivas de Orina, con el fin de promover una mayor participaci\u00f3n de oferentes. Esta modalidad de solicitud en un lote independiente ha sido adoptada en muchos de los llamados del MSPBS, y como referencia puede citarse la \u201cLPN N\u00ba 74/2024 - ADQUISICION DE REACTIVOS E INSUMOS PARA EL HOSPITAL NACIONAL\u201d, cuya complejidad es equiparable a la del presente llamado.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:41-04:00"}, {"id": "ac85b7fd076fc3ced68f6423d10fcaa0-1", "date": "2025-06-11T14:38:24-04:00", "title": "Lote 1 Equipo de Inmunoensayo", "description": "En el punto d. se solicita que \"El m\u00f3dulo de inmunolog\u00eda debe tener 70 reactivos a bordo m\u00ednimamente para cubrir la mayor cantidad de determinaciones\", mientras que en el punto ax. se especifica que \"el m\u00f3dulo de inmunolog\u00eda debe tener capacidad de 50 reactivos a bordo m\u00ednimamente para cubrir la mayor cantidad de determinaciones\". Agradecer\u00edamos que pudieran aclarar cu\u00e1l de las dos capacidades de reactivos a bordo para el m\u00f3dulo de inmunolog\u00eda es la requerida (70 o 50 reactivos). Esta clarificaci\u00f3n es importante para poder presentar una propuesta que se ajuste con precisi\u00f3n a sus expectativas.\nPara fomentar una mayor participaci\u00f3n y la libre competencia entre los oferentes, y considerando las capacidades est\u00e1ndar de muchos sistemas de inmunoensayo, sugerimos establecer una capacidad m\u00ednima de reactivos a bordo para el m\u00f3dulo de inmunolog\u00eda en el rango de 30 a 45 reactivos. Creemos que este rango es m\u00e1s razonable y permitir\u00eda la oferta de una gama m\u00e1s amplia de equipos de alto rendimiento disponibles en el mercado.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:43-04:00"}, {"id": "410b8c077211200db5db9e232222c8c1-1", "date": "2025-06-13T14:16:51-04:00", "title": "Lote 1 \u2013 Tiras de Orina", "description": "Solicitamos a la convocante considerar la separaci\u00f3n del \u00cdtem 83 del Lote 1, correspondiente a Tiras Reactivas de Orina, con el fin de promover una mayor participaci\u00f3n de oferentes. Esta modalidad de solicitud en un lote independiente ha sido adoptada en muchos de los llamados del MSPBS, y como referencia puede citarse la \u201cLPN N\u00b0 128/24 ID 453756 \u2013 ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA HOSPITALES GENERALES\u201d, cuya complejidad es equiparable a la del presente llamado.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:57-04:00"}, {"id": "e384c24e9ffeaec6893b61e447b506fe-1", "date": "2025-11-10T09:09:33-04:00", "title": "PLAN DE ENTREGA DE LOS BIENES", "description": "En el apartado de PLAN DE ENTREGA DE LOS BIENES, en el punto CANTIDADES M\u00c1XIMAS, donde menciona: \u201cConforme a la necesidad del servicio. El proveedor deber\u00e1 entregar el bien solicitado dentro de los 20 (veinte) d\u00edas calendario de haber retirado la Orden de Compra.\u201d Se solicita atentamente a la entidad convocante extender el plazo de entrega a 45 d\u00edas calendario, teniendo en cuenta que la modalidad de suministro ser\u00e1 conforme a las necesidades del servicio, por lo que no es posible conocer de antemano la cantidad exacta que se requerir\u00e1 ni planificar una producci\u00f3n espec\u00edfica con antelaci\u00f3n. Este plazo ampliado resulta necesario para contemplar los tiempos habituales de fabricaci\u00f3n, log\u00edstica internacional, procesos de importaci\u00f3n y tr\u00e1mites aduaneros, los cuales pueden superar f\u00e1cilmente los 30 d\u00edas, aun en condiciones operativas normales. Mantener el plazo actual podr\u00eda limitar injustificadamente la participaci\u00f3n de oferentes que no cuenten con stock inmediato, favoreciendo \u00fanicamente a quienes disponen de inventario local, lo cual introduce un sesgo competitivo contrario a los principios de igualdad, libre concurrencia y transparencia que deben regir los procesos de contrataci\u00f3n p\u00fablica. Por todo lo expuesto, se solicita que dicho requerimiento quede redactado de la siguiente manera: \u201cConforme a la necesidad del servicio. El proveedor deber\u00e1 entregar el bien solicitado dentro de los 45 (cuarenta y cinco) d\u00edas calendario de haber retirado la Orden de Compra.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:07:12-04:00"}, {"id": "9d79df3fc75e0761c1673cdcf5b6f861-1", "date": "2025-06-18T08:11:06-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 49, \u00edtem 1: (Test R\u00e1pido para Influenza), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con\n\n99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita amablemente a la entidad convocante considerar la admisi\u00f3n de pruebas r\u00e1pidas para detecci\u00f3n de Influenza A y B con una sensibilidad m\u00ednima del 87% y una especificidad m\u00ednima del 94%, par\u00e1metros que se encuentran dentro de los rangos internacionalmente aceptados para test de tamizaje o diagn\u00f3stico r\u00e1pido en entornos cl\u00ednicos y comunitarios. Tanto la sensibilidad del 87% como la especificidad del 94% garantizan una adecuada confiabilidad diagn\u00f3stica, especialmente para pruebas utilizadas en el primer nivel de atenci\u00f3n o en situaciones donde se requiere una detecci\u00f3n r\u00e1pida, accesible y operativamente eficiente. Estos valores son comunes y cl\u00ednicamente aceptables para pruebas de inmunoensayo cualitativas, seg\u00fan lo reportado en literatura cient\u00edfica y recomendaciones de organismos como la OMS. Adem\u00e1s, esta modificaci\u00f3n no compromete el objetivo sanitario del proceso ni la utilidad cl\u00ednica del test, pero s\u00ed ampl\u00eda la posibilidad de participaci\u00f3n de m\u00e1s oferentes, fomentando una mayor competencia en la adquisici\u00f3n p\u00fablica, sin perjuicio de la calidad del reactivo. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 87% de sensibilidad y 94% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:50:43-04:00"}, {"id": "7ad82672835c5c5c01206c503ecdc0b5-1", "date": "2025-06-11T14:40:53-04:00", "title": "LOTE 49 TEST RAPIDO PARA INFLUENZA", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas para TEST R\u00c1PIDO PARA INFLUENZA. Hemos notado que se solicitan valores de sensibilidad y especificidad muy elevados (99,9% y 99,6% respectivamente), los cuales son extremadamente exigentes para la categor\u00eda de tests r\u00e1pidos de influenza y podr\u00edan limitar severamente la participaci\u00f3n. Para asegurar una competencia justa y permitir la oferta de test r\u00e1pidos de influenza que son de uso com\u00fan y validados en la pr\u00e1ctica cl\u00ednica por su alta fiabilidad, solicitamos amablemente que se acepten test r\u00e1pidos con una sensibilidad mayor o igual a 99% y una especificidad mayor o igual a 98%.\nCreemos que estos valores representan un rendimiento diagn\u00f3stico superior y son m\u00e1s coherentes con la realidad del mercado de tests r\u00e1pidos, permitiendo la oferta de productos de calidad comprobada por un mayor n\u00famero de proveedores.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:35-04:00"}, {"id": "457baa5d73e5a7dfcdd53552b8445af7-1", "date": "2025-11-10T09:07:44-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita la modificaci\u00f3n en la descripci\u00f3n del producto, debido a que se ha detectado un error de tipeo en la siguiente frase: \u201cPara la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV.\u201d La redacci\u00f3n correcta deber\u00eda ser: \u201cPara la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del virus del Dengue.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones", "dateAnswered": "2025-11-11T11:42:49-04:00"}, {"id": "60d073775230ea35cc88d4759b9e4dc0-1", "date": "2025-06-09T17:11:56-04:00", "title": "Lote 44 Cronometro", "description": "Favor aclarar si est\u00e1n precisando TIMER para LABORATORIO \u00f3 Cronometro, debido a que en las especificaciones t\u00e9cnicas se refieren a Timer y no a Cronometro.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:46:49-04:00"}, {"id": "8f93671bea4848677fcbaf86afe773f7-1", "date": "2025-06-18T10:05:17-04:00", "title": "PLAN DE ENTREGA - REACTIVOS", "description": "El PBC establece CANTIDADES M\u00cdNIMAS:\n\n1RA. ENTREGA DE LA CANTIDAD M\u00cdNIMA (20%) : Una vez emitida la orden de compra por el administrador del contrato; el oferente tendr\u00e1 un plazo de hasta 5 (cinco) d\u00edas calendario para la entrega de los productos adjudicados a partir de la recepci\u00f3n de la Orden de Compra . Solicitamos a la Convocante analizar y extender el plazo de entrega de los bienes hasta un plazo de 20 (Veinte) d\u00edas calendarios, teniendo en cuenta el tiempo y la burocracia administrativa en la importaci\u00f3n de los bienes.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:01:21-04:00"}, {"id": "1af45a07ea7ae096f032b97b70e04c69-1", "date": "2025-06-10T15:45:59-04:00", "title": "Lote N\u00ba 14", "description": "Solicitamos encarecidamente a la convocante modificar el precio referencial a por lo menos a  6.000 Gs por determinaci\u00f3n, favor verificar los precios ofertados en licitaciones anteriores con vuestra instituci\u00f3n correspondiente al a\u00f1o 2024, para que no sea declarado desierto por la discrepancia que pudiera existir con el precio actual del mercado.", "answer": "La determinaci\u00f3n del precio referencial se realiz\u00f3 con la aplicaci\u00f3n de las metodolog\u00edas contempladas en la Resoluci\u00f3n DNCP N\u00b0 454/2024. El precio referencial no es restrictivo ni condicionante. ", "dateAnswered": "2025-11-11T11:45:33-04:00"}, {"id": "17007b43abb58ed3dc9b0b7d3883a2bf-1", "date": "2025-06-13T14:16:03-04:00", "title": "Capacidad t\u00e9cnica - Para PDIV", "description": "Se solicita amablemente tener en cuenta que la  transici\u00f3n de LCSP a DINAVISA es reciente, por lo que muchos productos a\u00fan se encuentran en tr\u00e1mite de Registro Sanitario. Se solicita admitir de forma extraordinaria, la Constancia de Tr\u00e1mite de Registro Sanitario, de la misma manera que se ha solicitado en los llamados LPN 130/2024 ID: 453781, LPN 155/2024 ID: 455249.: \"Constancia de Inscripci\u00f3n del PDIV (Productos para Diagnostico de Uso In Vitro) expedida por la Direcci\u00f3n de Registros, Habilitaci\u00f3n y Control del Laboratorio Central de Salud P\u00fablica o Registro Sanitario de DINAVISA seg\u00fan corresponda. En caso de que los documentos se encuentren vencidos deber\u00e1 acompa\u00f1ar la Constancia o Certificado de Tr\u00e1mite emitido por DINAVISA\", de tal forma a poder fomentar una mayor participaci\u00f3n de oferentes.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:48-04:00"}, {"id": "d1dbd37291ab206040cce893c1e7d4cb-1", "date": "2025-06-11T14:38:29-04:00", "title": "Lote 1. Equipo de Inmunoensayo", "description": "Solicitamos amablemente que se admita la posibilidad de complementar el equipo principal con un equipo de soporte adicional para el \u00e1rea de inmunoensayo, en caso de que el equipo principal no cubra la totalidad de las determinaciones requeridas.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:53-04:00"}, {"id": "58a0814ccfd0563f32a7ac6adef8c73a-1", "date": "2025-06-10T16:31:15-04:00", "title": "Lote N\u00ba 26", "description": "Solicitamos encarecidamente a la convocante modificar el precio referencial a por lo menos a  150.000 Gs la cajita x 10 unidades, favor verificar los precios ofertados en licitaciones anteriores con vuestra instituci\u00f3n correspondiente al a\u00f1o 2024, para que no sea declarado desierto por la discrepancia que pudiera existir con el precio actual del mercado.", "answer": "La determinaci\u00f3n del precio referencial se realiz\u00f3 con la aplicaci\u00f3n de las metodolog\u00edas contempladas en la Resoluci\u00f3n DNCP N\u00b0 454/2024. El precio referencial no es restrictivo ni condicionante.", "dateAnswered": "2025-11-11T11:45:44-04:00"}, {"id": "fdd909fb238466398ac278df96b0e87a-1", "date": "2025-06-13T14:17:13-04:00", "title": "Lote 1 \u2013 Cartucho Analizador de Sangre", "description": "Solicitamos a la convocante considerar la separaci\u00f3n del \u00cdtem 84 del Lote 1, correspondiente a Cartucho Analizador de Sangre, con el fin de promover una mayor participaci\u00f3n de oferentes. Esta modalidad de solicitud en un lote independiente ha sido adoptada en muchos de los llamados del MSPBS, y como referencia puede citarse la \u201cLPN N\u00b0 128/24 ID 453756 \u2013 ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA HOSPITALES GENERALES\u201d, cuya complejidad es equiparable a la del presente llamado.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:02-04:00"}, {"id": "5e7bbe0611941801aa3512e2e70ab631-1", "date": "2025-06-18T10:04:42-04:00", "title": "EQUIPOS EN COMODATO", "description": "El oferente contar\u00e1 con 45 (CUARENTA Y CINCO) d\u00edas calendario para la instalaci\u00f3n y puesta en marcha de los equipos a ser entregados en comodato, incluyendo el software de gesti\u00f3n (con todos los reportes) solicitado, contados a partir de la recepci\u00f3n del contrato respectivo por parte del proveedor. Solicitamos a la Convocante extender el plazo de entrega, instalaci\u00f3n y puesta en marca de los equipos a por lo menos 90 (NOVENTA) d\u00edas calendarios, teniendo en cuenta el tiempo y la burocracion en el tramite de importacion de los mismos,", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:01:13-04:00"}, {"id": "54a760ea51653c50d2457d32df6cf1d0-1", "date": "2025-11-10T09:07:27-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita respetuosamente a la entidad convocante aceptar pruebas r\u00e1pidas para la detecci\u00f3n de Dengue ant\u00edgeno NS1 y anticuerpos IgG/IgM que presenten una sensibilidad m\u00ednima del 95% y una especificidad m\u00ednima del 96%. Estos valores se encuentran dentro de los rangos com\u00fanmente aceptados a nivel internacional para pruebas de tamizaje serol\u00f3gico y de ant\u00edgeno, utilizadas en contextos cl\u00ednicos y comunitarios. Tanto la sensibilidad del 95% como la especificidad del 96% aseguran una confiabilidad diagn\u00f3stica adecuada, especialmente en situaciones donde se requiere una detecci\u00f3n r\u00e1pida y efectiva, como en el primer nivel de atenci\u00f3n y en zonas con alta circulaci\u00f3n viral. Estos valores son frecuentes y considerados cl\u00ednicamente v\u00e1lidos en pruebas r\u00e1pidas de inmunoensayo cualitativas, seg\u00fan la literatura cient\u00edfica y las recomendaciones de organismos internacionales como la Organizaci\u00f3n Mundial de la Salud (OMS) y la Organizaci\u00f3n Panamericana de la Salud (OPS). Esta modificaci\u00f3n no compromete la eficacia cl\u00ednica del test requerido, pero favorece a una mayor participaci\u00f3n de oferentes, lo que promueve un proceso de adquisici\u00f3n m\u00e1s competitivo y equitativo, sin afectar la calidad del reactivo ni su desempe\u00f1o diagn\u00f3stico. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 95% de sensibilidad y 96% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:37:20-04:00"}, {"id": "58d25af9d01cf26a6da987383764b0ff-1", "date": "2025-06-11T14:40:48-04:00", "title": "LOTE 48 TEST R\u00c1PIDO PARA ROTAVIRUS", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas TEST R\u00c1PIDO PARA ROTAVIRUS, con el fin de ampliar la base de posibles oferentes y permitir la inclusi\u00f3n de test r\u00e1pidos de rotavirus que son ampliamente reconocidos por su excelente rendimiento cl\u00ednico, solicitamos amablemente que se acepte una sensibilidad mayor o igual a 99% y una especificidad mayor o igual a 98%.\nConsideramos que estos umbrales garantizan un alto nivel de fiabilidad diagn\u00f3stica, siendo representativos de tests r\u00e1pidos de alta calidad disponibles en el mercado, y permitir\u00edan una competencia m\u00e1s equitativa.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:23-04:00"}, {"id": "237d06f18b7938443c857e48f105fb6e-1", "date": "2025-06-11T14:38:24-04:00", "title": "Lote 1. Equipo de Inmunoensayo", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas para el m\u00f3dulo de inmunoensayo. Espec\u00edficamente, en el punto g. se indica \"M\u00f3dulo de inmunoensayo que utilice puntas de muestra desechables para la eliminaci\u00f3n del arrastre\". Agradecer\u00edamos que pudieran considerar la posibilidad de que el m\u00f3dulo de inmunoensayo tambi\u00e9n admita el uso de puntas lavables que cuenten con un sistema de lavado y desinfecci\u00f3n eficaz para la eliminaci\u00f3n del arrastre. Esta alternativa podr\u00eda ofrecer ventajas en t\u00e9rminos de costos operativos y sostenibilidad ambiental, sin comprometer la precisi\u00f3n de los resultados, siempre y cuando el sistema de lavado garantice la ausencia de arrastre.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:50-04:00"}, {"id": "cde0536580a63407f68cd7cf1d0235bf-1", "date": "2025-11-10T09:04:33-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de ESPECIFICACIONES T\u00c9CNICAS, en el lote 48, \u00edtem 1: (Test R\u00e1pido para Rotavirus), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99 % de sensibilidad y 99 % de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita a la convocante admitir una sensibilidad del 97% como m\u00ednimo ya que esta sensibilidad sigue siendo altamente efectiva para pruebas de tamizaje, y es la sensibilidad m\u00e1s com\u00fan para estos tipos de test. Al establecer este est\u00e1ndar, se facilitar\u00e1 la participaci\u00f3n de un mayor n\u00famero de oferentes, lo que promover\u00e1 la competencia y, potencialmente, mejores condiciones en la adquisici\u00f3n de los productos. Por lo tanto, proponemos que dicho requerimiento se redacte de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 97% de sensibilidad y 99% de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:33:39-04:00"}, {"id": "71dcf52f6fec5f81eec76471b5b7e7f4-1", "date": "2025-11-10T09:03:20-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 41, \u00edtem 1 (PIPETA PASTEUR), donde dice: \u201cDE PLASTICO, DE 5 ML DE VOLUMEN.\u201d Se solicita amablemente a la convocante considerar la aceptaci\u00f3n de un volumen de 12 mililitros, con una escala de graduaci\u00f3n que var\u00eda de 1 a 5 ml, dado que este rango incluye el volumen requerido y proporciona una mayor flexibilidad. Esto facilita el trabajo en laboratorio y permite una adaptabilidad superior en los procedimientos. Por lo expuesto, solicitamos que dicho enunciado quede redactado de la siguiente forma: \u201cDE PLASTICO, DE 5 ML DE VOLUMEN COMO M\u00cdNIMO.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones", "dateAnswered": "2025-11-11T11:25:34-04:00"}, {"id": "d1d35d78223214b568e2fdd6e06fcca8-1", "date": "2025-06-18T08:08:23-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 34, \u00edtem 1 (L\u00c1MINAS PORTAOBJETO), donde dice: \u201cDe vidrio, m\u00ednimas dimensiones 74 x 24 (+/-1) mm. en caja x 50 unidades como m\u00ednimo. Trasl\u00facidas, libre de ralladuras y que no se peguen entre s\u00ed. Oferta es por unidad individual de l\u00e1mina. Presentaci\u00f3n de entrega: Caja de 50 unidades como m\u00ednimo.\u201d Se solicita amablemente a la convocante considerar la admisi\u00f3n de l\u00e1minas lisas, ya que ofrecen una observaci\u00f3n clara y sin distorsiones, permitiendo\n\nvisualizar detalles finos y con alta resoluci\u00f3n al no alterar la trayectoria de la luz que atraviesa la muestra. Adem\u00e1s, son compatibles con una amplia variedad de t\u00e9cnicas de microscop\u00eda, incluidas la microscop\u00eda de campo claro y de contraste de fases. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cDe vidrio, m\u00ednimas dimensiones 74 x 24 (+/-1) mm. en caja x 50 unidades como m\u00ednimo. Trasl\u00facidas o lisas, libre de ralladuras y que no se peguen entre s\u00ed. Oferta es por unidad individual de l\u00e1mina. Presentaci\u00f3n de entrega: Caja de 50 unidades como m\u00ednimo.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:49-04:00"}, {"id": "31905f677c1f86c50ccca0c31e7928ef-1", "date": "2025-06-09T16:41:31-04:00", "title": "Lote N\u00ba 20", "description": "\u00bfPodemos ofertar en una presentaci\u00f3n de caja x 24 test como m\u00ednimo?", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:46:41-04:00"}, {"id": "3c8e5b56da2270f0f1e0cfc088c1508c-1", "date": "2025-06-18T08:13:02-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 20, \u00edtem 1: (TEST PARA SANGRE OCULTA), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. M\u00e9todo inmunol\u00f3gico para la detecci\u00f3n de hemoglobina en las heces frescas. Presentaci\u00f3n de entrega: Capacidad de realizar entre 25 y 50 determinaciones por presentaci\u00f3n.\u201d Se solicita amablemente a la convocante admitir una presentaci\u00f3n de 20 determinaciones por caja como m\u00ednimo, ya que esto no afecta la finalidad de uso del test ni compromete su efectividad. Adem\u00e1s, se respetar\u00eda el n\u00famero total de pruebas solicitadas, garantizando el cumplimiento de los requerimientos sin alterar el objetivo del proceso. Esta modificaci\u00f3n tambi\u00e9n favorecer\u00eda la participaci\u00f3n de un mayor n\u00famero de oferentes, promoviendo un proceso m\u00e1s justo y transparente para todos. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. M\u00e9todo inmunol\u00f3gico para la detecci\u00f3n de hemoglobina en las heces frescas. Presentaci\u00f3n de entrega: Capacidad de realizar entre 20 y 50 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:52:16-04:00"}, {"id": "3f848aeec3d46ba670cbe37aaa0f83dc-1", "date": "2025-06-18T08:11:26-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita la modificaci\u00f3n en la descripci\u00f3n del producto, debido a que se ha detectado un error de tipeo en la siguiente frase: \u201cPara la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV.\u201d La redacci\u00f3n correcta deber\u00eda ser: \u201cPara la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del virus del Dengue.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:51:16-04:00"}, {"id": "36206406865a2c830d5ac66a55356cd6-1", "date": "2025-06-13T14:17:24-04:00", "title": "Lote 1 \u2013 Cartucho Analizador de Sangre", "description": "Solicitamos a la convocante considerar la separaci\u00f3n del \u00cdtem 84 del Lote 1, correspondiente a Cartucho Analizador de Sangre, con el fin de promover una mayor participaci\u00f3n de oferentes. Esta modalidad de solicitud en un lote independiente ha sido adoptada en muchos de los llamados del MSPBS, y como referencia puede citarse \u201cLPN 134/24 ID.: 454374\u2013 ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA EL INSTITUTO DE MEDICINA TROPICAL\u201d, cuya complejidad es equiparable a la del presente llamado.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:38-04:00"}, {"id": "5d7879d357392511a4aaca0a07de01fc-1", "date": "2025-11-10T09:02:19-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de ESPECIFICACIONES T\u00c9CNICAS, en el lote 19, \u00edtem 1: (Test R\u00e1pido para Rotavirus), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d Se solicita a la convocante admitir una sensibilidad del 98% como m\u00ednimo ya que esta sensibilidad sigue siendo altamente efectiva para pruebas de tamizaje, y es la sensibilidad m\u00e1s com\u00fan para estos tipos de test. Al establecer este est\u00e1ndar, se facilitar\u00e1 la participaci\u00f3n de un mayor n\u00famero de oferentes, lo que promover\u00e1 la competencia y, potencialmente, mejores condiciones en la adquisici\u00f3n de los productos. Por lo tanto, proponemos que dicho requerimiento se redacte de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 98% como m\u00ednimo de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:29:27-04:00"}, {"id": "81644759965bebe31da49be08582adf8-1", "date": "2025-11-10T09:13:21-04:00", "title": "An\u00e1lisis de precios ofertados", "description": "Seg\u00fan Resoluci\u00f3n DNCP N\u00ba 454/2024 Art. 4to. se determina que:\n(\u2026) En contrataciones en general: cuando la diferencia entre el precio ofertado y el precio referencial sea superior al 25% para ofertas por debajo del precio referencial y del 15% para ofertas que se encuentren por encima del referencial establecido por la convocante y difundido con el llamado a contrataci\u00f3n.\n\nSeg\u00fan Informe de Evaluaci\u00f3n de la licitaci\u00f3n N\u00ba 127/2024 ID N\u00ba 453750 cuya apertura se realiz\u00f3 en fecha 26/11/2024 pueden observarse, que algunos lotes fueron adjudicados con m\u00e1rgenes tanto inferior como superior, del 35 %, respecto a los precios referenciales.\n\nTambi\u00e9n, por ejemplo, seg\u00fan Informe de Evaluaci\u00f3n de la licitaci\u00f3n N\u00ba 128/2024 ID N\u00ba 453756 cuya apertura se realiz\u00f3 en fecha 27/03/2025 pueden observarse que fueron aceptadas ofertas con precios de hasta 50% por debajo y de hasta 35 % por arriba de los precios referenciales respectivos.\n\nConsulta: Teniendo en cuenta lo antedicho en los p\u00e1rrafos anteriores y para no trabajar en vano, consultamos cu\u00e1l de las siguientes f\u00f3rmulas ( -25% hasta +15%, -35% hasta +35% \u00f3 -50% hasta +35% ) \u00bf ser\u00e1n entonces aceptadas/respetadas en esta licitaci\u00f3n ?", "answer": "La Convocante requerir\u00e1 desglose de precios duando la diferencia entre el precio ofertado y el precio referencial sea superior al 25% para ofertas por debajo del precio referencial y del 15% para ofertas que se encuentren por encima del referencialen caso que el precio ofertado no se ajuste al rango del -25% + 15%, donde el Comit\u00e9 de Evaluaci\u00f3n analizar\u00e1 la composici\u00f3n y concluir\u00e1 al respecto.", "dateAnswered": "2025-11-11T11:04:29-04:00"}, {"id": "991b4fcfb62ce7f294ec70d15aafa1e3-1", "date": "2025-11-10T09:01:42-04:00", "title": "Vencimiento de Insumos de Laboratorio Inertes", "description": "Favor considerar la entrega sin lote y sin vencimientos de los Productos ( INSUMOS DE LABORATORIO ) considerados INERTES debido a la naturaleza del mismo, para los lotes 23, 24, 25, 26, 27, 28, 29, 32, 33, 34, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45 y 46", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:28:41-04:00"}, {"id": "2dc3a699e776c2ccc8a5a3daa6202dc1-1", "date": "2025-11-10T09:09:47-04:00", "title": "VENCIMIENTOS PERIODO DE VALIDEZ DE GARANTIA DE LOS BIENES", "description": "En el apartado de VENCIMIENTOS PERIODO DE VALIDEZ DE GARANTIA DE LOS BIENES, donde menciona: \u201cEl vencimiento de los productos debe ser igual o superior a 12 (doce) meses al momento de la entrega en el lugar indicado, si por la naturaleza del mismo o por necesidad de la Instituci\u00f3n no se puede cumplir con este requisito, la recepci\u00f3n del articulo deber\u00e1 ser autorizada por el Administrador del Contrato con previa conformidad de Servicio de Laboratorio beneficiado; adem\u00e1s se deber\u00e1 presentar Carta Compromiso de Canje, una p\u00f3liza de Seguro por el 100 % del monto del producto con identificaci\u00f3n del n\u00famero de lote. La validez de dicha p\u00f3liza deber\u00e1 ser por 3 meses posteriores a la fecha del vencimiento del art\u00edculo a entregar.\u201d Se solicita atentamente a la entidad convocante esclarecer el criterio aplicable al per\u00edodo de validez de los productos incluidos en los lotes N.\u00ba 23, 27, 28, 29, 30, 32, 33, 34, 37, 38, 39, 40, 41, 43, 45 y 46, considerando que dichos lotes contienen insumos de distinta naturaleza. En particular, se destaca que los productos de vidrier\u00eda de laboratorio (como tubos de ensayo, vasos precipitados, probetas, etc.) no poseen fecha de vencimiento, ya que son bienes durables y reutilizables bajo condiciones normales de uso y esterilizaci\u00f3n. En cambio, las pipetas automatizadas o equipos de medici\u00f3n s\u00ed pueden tener un per\u00edodo de validez o vida \u00fatil limitada, determinado por el fabricante, asociado al uso continuo, calibraci\u00f3n y mantenimiento. Por lo tanto, se solicita aclarar si el requerimiento de vigencia m\u00ednima aplica a todos los productos de estos lotes por igual, o si se evaluar\u00e1 de acuerdo con la naturaleza t\u00e9cnica de cada insumo, a fin de evitar interpretaciones err\u00f3neas.", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:33:02-04:00"}, {"id": "803f5b5d6833715e353d8b824367e644-1", "date": "2025-06-18T08:10:04-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de ESPECIFICACIONES T\u00c9CNICAS, en el lote 48, \u00edtem 1: (Test R\u00e1pido para Rotavirus), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99 % de sensibilidad y 99 % de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita a la convocante admitir una sensibilidad del 97% como m\u00ednimo ya que esta sensibilidad sigue siendo altamente efectiva para pruebas de tamizaje, y es la sensibilidad m\u00e1s com\u00fan para estos tipos de test. Al establecer este est\u00e1ndar, se facilitar\u00e1 la participaci\u00f3n de un mayor n\u00famero de oferentes, lo que promover\u00e1 la competencia y, potencialmente, mejores condiciones en la adquisici\u00f3n de los productos. Por lo tanto, proponemos que dicho requerimiento se\n\nredacte de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 97% de sensibilidad y 99% de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:50:07-04:00"}, {"id": "821cf6657901bf2af61d4a12ccfa01b1-1", "date": "2025-06-18T08:11:22-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del\n\npa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita respetuosamente a la entidad convocante aceptar pruebas r\u00e1pidas para la detecci\u00f3n de Dengue ant\u00edgeno NS1 y anticuerpos IgG/IgM que presenten una sensibilidad m\u00ednima del 95% y una especificidad m\u00ednima del 96%. Estos valores se encuentran dentro de los rangos com\u00fanmente aceptados a nivel internacional para pruebas de tamizaje serol\u00f3gico y de ant\u00edgeno, utilizadas en contextos cl\u00ednicos y comunitarios. Tanto la sensibilidad del 95% como la especificidad del 96% aseguran una confiabilidad diagn\u00f3stica adecuada, especialmente en situaciones donde se requiere una detecci\u00f3n r\u00e1pida y efectiva, como en el primer nivel de atenci\u00f3n y en zonas con alta circulaci\u00f3n viral. Estos valores son frecuentes y considerados cl\u00ednicamente v\u00e1lidos en pruebas r\u00e1pidas de inmunoensayo cualitativas, seg\u00fan la literatura cient\u00edfica y las recomendaciones de organismos internacionales como la Organizaci\u00f3n Mundial de la Salud (OMS) y la Organizaci\u00f3n Panamericana de la Salud (OPS). Esta modificaci\u00f3n no compromete la eficacia cl\u00ednica del test requerido, pero favorece a una mayor participaci\u00f3n de oferentes, lo que promueve un proceso de adquisici\u00f3n m\u00e1s competitivo y equitativo, sin afectar la calidad del reactivo ni su desempe\u00f1o diagn\u00f3stico. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 95% de sensibilidad y 96% de especificidad como m\u00ednimo. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:51:11-04:00"}, {"id": "710de3df1931af653c680601715a7e7c-1", "date": "2025-06-13T09:33:10-04:00", "title": "LOTE 47 - ITEM 01", "description": "Se consulta amablemente si podr\u00eda ofertarse un test r\u00e1pido para Chagas con sensibilidades aproximadas a 96,4% en sangre entera capilar, 95,1% sangre entera venosa, 92,2% con muestras de suero y con especificidades de 96% en sangre entera capilar, 98,3% de sangre entera venosa y 98,5 % en muestras de suero. De esta manera se podr\u00eda ampliar la cantidad de oferentes y tener mejores ofertas presentadas en la apertura del llamado. El rango solicitado actualmente limita mucho la participaci\u00f3n teniendo en cuenta que las marcas presentes en el mercado poseen un rango de sensibilidad y especificidad m\u00e1s amplio.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:40-04:00"}, {"id": "7caddd725faa40382915700364a3516a-1", "date": "2025-06-18T08:10:58-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 49, \u00edtem 1: (Test R\u00e1pido para Influenza), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita respetuosamente a la entidad convocante considerar la admisi\u00f3n de presentaciones de 20 determinaciones por caja como m\u00ednimo, en lugar del formato especificado, siempre que se mantenga el total de determinaciones requeridas en el pliego. Esta modificaci\u00f3n no afecta la finalidad de uso del test ni compromete su efectividad diagn\u00f3stica. Adem\u00e1s, esta flexibilizaci\u00f3n permitir\u00eda ampliar la base de oferentes potenciales, fomentando una mayor competencia y transparencia en el proceso de adquisici\u00f3n.Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:50:33-04:00"}, {"id": "620f32b7b9aa998bd79a3fa00d07f6aa-1", "date": "2025-06-18T08:12:01-04:00", "title": "PLAN DE ENTREGA DE LOS BIENES", "description": "En el apartado de PLAN DE ENTREGA DE LOS BIENES, en el punto CANTIDADES M\u00c1XIMAS, donde menciona: \u201cConforme a la necesidad del servicio. El proveedor deber\u00e1 entregar el bien solicitado dentro de los 20 (veinte) d\u00edas calendario de haber retirado la Orden de Compra.\u201d Se solicita atentamente a la entidad convocante extender el plazo de entrega a 45 d\u00edas calendario, teniendo en cuenta que la modalidad de suministro ser\u00e1 conforme a las necesidades del servicio, por lo que no es posible conocer de antemano la cantidad exacta que se requerir\u00e1 ni planificar una producci\u00f3n espec\u00edfica con antelaci\u00f3n. Este plazo ampliado resulta necesario para contemplar los tiempos habituales de fabricaci\u00f3n, log\u00edstica internacional, procesos de importaci\u00f3n y tr\u00e1mites aduaneros, los cuales pueden superar f\u00e1cilmente los 30 d\u00edas, aun en condiciones operativas normales. Mantener el plazo actual podr\u00eda limitar injustificadamente la participaci\u00f3n de oferentes que no cuenten con stock inmediato, favoreciendo \u00fanicamente a quienes disponen de inventario local, lo cual introduce un sesgo competitivo contrario a los principios de igualdad, libre concurrencia y transparencia que deben regir los procesos de contrataci\u00f3n p\u00fablica. Por todo lo expuesto,\n\nse solicita que dicho requerimiento quede redactado de la siguiente manera: \u201cConforme a la necesidad del servicio. El proveedor deber\u00e1 entregar el bien solicitado dentro de los 45 (cuarenta y cinco) d\u00edas calendario de haber retirado la Orden de Compra.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:52:08-04:00"}, {"id": "20865c2c4cbb54868c22319ebb28a9fc-1", "date": "2025-06-18T10:04:26-04:00", "title": "PORCENTAJE DE MULTA", "description": "Solicitamos a la Convocante analizar y unificar el porcentaje de multa a 0,001%, tal como lo establece el porcentaje de tasa de inter\u00e9s de mora por parte de la contratante, a fin de lograr una igualdad de condiciones en el pliego de bases y condiciones.", "answer": "El porcentaje de multa se establece como penalizaci\u00f3n de la demora en la entrega de los productos, considerando el da\u00f1o o perjuicio que podr\u00eda implicar para la Instituci\u00f3n y pacientes oncol\u00f3gicos. El porcentaje de tasa de inter\u00e9s por mora por parte de la Contratante se remite a una pol\u00edtica institucional que puede verificarse en las convocatorias del MInisterio de Salud P\u00fablica y Bienestar Social, ente rector. Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:56:01-04:00"}, {"id": "8c223ddae3fa3377771bbce248a24d5b-1", "date": "2025-06-11T14:40:44-04:00", "title": "LOTE 34 L\u00c1MINA PORTAOBJETOS", "description": "La convocante solicita una medida de 74 x 24 (+/-1) mm de l\u00e1mitas portaobjeto. Para fomentar una mayor competencia y permitir la oferta de l\u00e1minas est\u00e1ndar de alta calidad disponibles en el mercado internacional, solicitamos amablemente que se acepte la medida de 74 x 24 (+/-2) mm. Esta tolerancia de +/-2 mm es com\u00fanmente aceptada en la industria para l\u00e1minas portaobjetos y no afectar\u00eda la funcionalidad, el rendimiento o la compatibilidad con los equipos de laboratorio existentes, mientras que ampliar\u00eda significativamente la gama de productos elegibles.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:48:14-04:00"}, {"id": "501288f5cdc96cc0d215e1371e1bccb3-1", "date": "2025-11-10T09:03:06-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 34, \u00edtem 1 (L\u00c1MINAS PORTAOBJETO), donde dice: \u201cDe vidrio, m\u00ednimas dimensiones 74 x 24 (+/-1) mm. en caja x 50 unidades como m\u00ednimo. Trasl\u00facidas, libre de ralladuras y que no se peguen entre s\u00ed. Oferta es por unidad individual de l\u00e1mina. Presentaci\u00f3n de entrega: Caja de 50 unidades como m\u00ednimo.\u201d Se solicita amablemente a la convocante considerar la admisi\u00f3n de l\u00e1minas lisas, ya que ofrecen una observaci\u00f3n clara y sin distorsiones, permitiendo\n\nvisualizar detalles finos y con alta resoluci\u00f3n al no alterar la trayectoria de la luz que atraviesa la muestra. Adem\u00e1s, son compatibles con una amplia variedad de t\u00e9cnicas de microscop\u00eda, incluidas la microscop\u00eda de campo claro y de contraste de fases. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cDe vidrio, m\u00ednimas dimensiones 74 x 24 (+/-1) mm. en caja x 50 unidades como m\u00ednimo. Trasl\u00facidas o lisas, libre de ralladuras y que no se peguen entre s\u00ed. Oferta es por unidad individual de l\u00e1mina. Presentaci\u00f3n de entrega: Caja de 50 unidades como m\u00ednimo.\u201d", "answer": "REmitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:31:03-04:00"}, {"id": "7995dc7d4f1180f5f8e6d180efd81c19-1", "date": "2025-06-09T16:39:43-04:00", "title": "Lotes N\u00ba 40, 41 y 42", "description": "Solicitamos a la convocante aclarar que est\u00e1n precisando realmente en estos lotes ya que existe una discrepancia entre el PBC y la planilla de precios.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:46:22-04:00"}, {"id": "4da56f5d0d2bc3b33c2543fdc8ee6494-1", "date": "2025-06-18T08:11:13-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 50, \u00edtem 1: Test R\u00e1pido para DENGUE (Ag + Ac), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita cordialmente a la entidad convocante aceptar presentaciones que contengan un m\u00ednimo de 20 determinaciones por caja, siempre que se garantice el cumplimiento del n\u00famero total de pruebas requerido en el pliego. Esta modificaci\u00f3n no afecta la utilidad ni la eficacia del test en su aplicaci\u00f3n diagn\u00f3stica. Asimismo, esta medida contribuir\u00eda a ampliar la participaci\u00f3n de oferentes, promoviendo un proceso de adquisici\u00f3n m\u00e1s competitivo, inclusivo y transparente. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa de ant\u00edgeno NS1 y anticuerpos IgG, IgM in vitro de anticuerpos del HCV. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:50:55-04:00"}, {"id": "8d1bf73ea3d0405805e0dcedf7602067-1", "date": "2025-06-11T14:38:10-04:00", "title": "LOTE 1; ITEM1 Equipo de Hemogramas", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas para la licitaci\u00f3n. Hemos notado que en el punto 1.j. se solicita una \"Velocidad de procesamiento: 120 muestras/hora como m\u00ednimo\", mientras que en el punto 5. se indica que \"El equipo debe procesar un m\u00ednimo de 80 muestras por hora\". Agradecer\u00edamos que pudieran aclarar cu\u00e1l de las dos velocidades de procesamiento es la requerida para el equipo, si 120 muestras/hora o 80 muestras/hora. Para fomentar una mayor participaci\u00f3n y ofrecer flexibilidad a los oferentes, sugerimos establecer una velocidad de procesamiento m\u00ednima de 80 a 100 muestras/hora, ya que esta permitir\u00eda que un rango m\u00e1s amplio de equipos de alto rendimiento pueda ser considerado.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:20-04:00"}, {"id": "4c2426410d37c0be57897e9ce2f1a2d8-1", "date": "2025-11-10T08:58:24-04:00", "title": "Lote 11 ASO", "description": "\u00bf Podemos presentar certificado de libre venta de origen en vez de certificado de calidad ?", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones", "dateAnswered": "2025-11-11T11:28:14-04:00"}, {"id": "935422866aa8f9976c3a5f9928e8a996-1", "date": "2025-06-18T08:11:46-04:00", "title": "VENCIMIENTOS PERIODO DE VALIDEZ DE GARANTIA DE LOS BIENES", "description": "En el apartado de VENCIMIENTOS PERIODO DE VALIDEZ DE GARANTIA DE LOS BIENES, donde menciona: \u201cEl vencimiento de los productos debe ser igual o superior a 12 (doce) meses al momento de la entrega en el lugar indicado, si por la naturaleza del mismo o por necesidad de la Instituci\u00f3n no se puede cumplir con este requisito, la recepci\u00f3n del articulo deber\u00e1 ser autorizada por el Administrador del Contrato con previa conformidad de Servicio de Laboratorio beneficiado; adem\u00e1s se deber\u00e1 presentar Carta Compromiso de Canje, una p\u00f3liza de Seguro por el 100 % del monto del producto con identificaci\u00f3n del n\u00famero de lote. La validez de dicha p\u00f3liza deber\u00e1 ser por 3 meses posteriores a la fecha del vencimiento del art\u00edculo a entregar.\u201d Se solicita atentamente a la entidad convocante esclarecer el criterio aplicable al per\u00edodo de validez de los productos incluidos en los lotes N.\u00ba 23, 27, 28, 29, 30, 32, 33, 34, 37, 38, 39, 40, 41, 43, 45 y 46, considerando que dichos lotes contienen insumos de distinta naturaleza. En particular, se destaca que los productos de vidrier\u00eda de laboratorio (como tubos de ensayo, vasos precipitados, probetas, etc.) no poseen fecha de vencimiento, ya que son bienes durables y reutilizables bajo condiciones normales de uso y esterilizaci\u00f3n. En cambio, las pipetas automatizadas o equipos de medici\u00f3n s\u00ed pueden tener un per\u00edodo de validez o vida \u00fatil limitada, determinado por el fabricante, asociado al uso continuo, calibraci\u00f3n y mantenimiento. Por lo tanto, se solicita aclarar si el requerimiento de vigencia m\u00ednima aplica a todos los productos de estos lotes por igual, o si se evaluar\u00e1 de acuerdo con la naturaleza t\u00e9cnica de cada insumo, a fin de evitar interpretaciones err\u00f3neas.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:52:02-04:00"}, {"id": "73fb200571432fc24a26024e4046efd0-1", "date": "2025-06-18T08:08:01-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de ESPECIFICACIONES T\u00c9CNICAS, en el lote 19, \u00edtem 1: (Test R\u00e1pido para Rotavirus), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d Se solicita a la convocante admitir una sensibilidad del 98% como m\u00ednimo ya que esta sensibilidad sigue siendo altamente efectiva para pruebas de tamizaje, y es la sensibilidad m\u00e1s com\u00fan para estos tipos de test. Al establecer este est\u00e1ndar, se facilitar\u00e1 la participaci\u00f3n de un mayor n\u00famero de oferentes, lo que promover\u00e1 la competencia y, potencialmente, mejores condiciones en la adquisici\u00f3n de los productos. Por lo tanto, proponemos que dicho requerimiento se redacte de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 98% como m\u00ednimo de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:44-04:00"}, {"id": "81d1cf7ccaf70f126eaddb4e5bf11339-1", "date": "2025-06-18T08:08:53-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 41, \u00edtem 1 (PIPETA PASTEUR), donde dice: \u201cDE PLASTICO, DE 5 ML DE VOLUMEN.\u201d Se solicita amablemente a la convocante considerar la aceptaci\u00f3n de un volumen de 12 mililitros, con una escala de graduaci\u00f3n que var\u00eda de 1 a 5 ml, dado que este rango incluye el volumen requerido y proporciona una mayor flexibilidad. Esto facilita el trabajo en laboratorio y permite una adaptabilidad superior en los procedimientos. Por lo expuesto, solicitamos que dicho enunciado quede redactado de la siguiente forma: \u201cDE PLASTICO, DE 5 ML DE VOLUMEN COMO M\u00cdNIMO.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:49:54-04:00"}, {"id": "6edb67afe879ee92ce95cdc53a74a5e1-1", "date": "2025-11-10T08:59:59-04:00", "title": "Lote 13 PCR", "description": "\u00bf Podemos presentar certificado de libre venta de origen en vez de certificado de calidad ?", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:24:55-04:00"}, {"id": "5449565acb089ef020dcc8424c3ec483-1", "date": "2025-06-11T14:38:19-04:00", "title": "LOTE 1. Equipo de qu\u00edmica cl\u00ednica", "description": "En relaci\u00f3n con las especificaciones t\u00e9cnicas para un equipo de qu\u00edmica-cl\u00ednica Hemos encontrado una especificaci\u00f3n que requiere \"Capacidad de procesar peque\u00f1os vol\u00famenes de muestras (desde 0,4\u03bcl. solicitamos aclaraci\u00f3n sobre este requisito de volumen de muestra. Un volumen de 0,4\u03bcl es excepcionalmente bajo y, desde un punto de vista pr\u00e1ctico en la qu\u00edmica cl\u00ednica, podr\u00eda generar errores significativos o no ser representativo para un an\u00e1lisis fiable debido a las limitaciones de pipeteo, evaporaci\u00f3n y la homogeneidad de la muestra en vol\u00famenes tan peque\u00f1os. Esta especificaci\u00f3n no parece tener un sentido pr\u00e1ctico para el procesamiento de la mayor\u00eda de las pruebas de qu\u00edmica cl\u00ednica y limitar\u00eda severamente la disponibilidad de equipos adecuados en el mercado. Agradecer\u00edamos que pudieran confirmar si este volumen de 0,4\u03bcl es correcto, o si se trata de un error tipogr\u00e1fico. En caso de ser un error, solicitamos que se especifique el volumen m\u00ednimo de muestra real y t\u00e9cnicamente viable requerido para el an\u00e1lisis en el equipo de qu\u00edmica.", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:47:37-04:00"}, {"id": "b57dfae4feaf27ec593508e0cdc60221-1", "date": "2025-11-10T09:05:04-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 49, \u00edtem 1: (Test R\u00e1pido para Influenza), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita respetuosamente a la entidad convocante considerar la admisi\u00f3n de presentaciones de 20 determinaciones por caja como m\u00ednimo, en lugar del formato especificado, siempre que se mantenga el total de determinaciones requeridas en el pliego. Esta modificaci\u00f3n no afecta la finalidad de uso del test ni compromete su efectividad diagn\u00f3stica. Adem\u00e1s, esta flexibilizaci\u00f3n permitir\u00eda ampliar la base de oferentes potenciales, fomentando una mayor competencia y transparencia en el proceso de adquisici\u00f3n. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de influenza A y B en hisopado nasofar\u00edngeo. Con 99,9% de sensibilidad y 99,6 % de especificidad. Con certificado de calidad del pa\u00eds de origen. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a las disposiciones del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T11:34:52-04:00"}, {"id": "2354e4c05b0273db5a4ef624e2ebb00f-1", "date": "2025-06-18T08:10:52-04:00", "title": "ESPECIFICACIONES TECNICAS", "description": "En el apartado de especificaciones t\u00e9cnicas, en el lote 48, \u00edtem 1: (Test R\u00e1pido para Rotavirus), donde dice: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99 % de sensibilidad y 99 % de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 25 determinaciones por presentaci\u00f3n.\u201d Se solicita amablemente a la convocante admitir una presentaci\u00f3n de 20 determinaciones por caja como m\u00ednimo, ya que esto no afecta la finalidad de uso del test ni compromete su efectividad. Adem\u00e1s, se respetar\u00eda el n\u00famero total de pruebas solicitadas, garantizando el cumplimiento de los requerimientos sin alterar el objetivo del proceso. Esta modificaci\u00f3n tambi\u00e9n favorecer\u00eda la participaci\u00f3n de un mayor n\u00famero de oferentes, promoviendo un proceso m\u00e1s justo y transparente para todos. Por lo expuesto, solicitamos que dicho requerimiento quede redactado de la siguiente manera: \u201cTest r\u00e1pido inmunocromatogr\u00e1fico en un solo paso. Para la detecci\u00f3n cualitativa in vitro de ant\u00edgenos de rotavirus en materia fecal humana. Con 99 % de sensibilidad y 99 % de especificidad como m\u00ednimo. Presentaci\u00f3n de entrega: Capacidad de realizar un m\u00ednimo de 20 determinaciones por presentaci\u00f3n.\u201d", "answer": "Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-11T10:50:11-04:00"}], "lots": [{"id": "1f007351-080a-64a6-bdce-0d7d5a7bb5ac", "title": "43 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 588000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "43"}]}, {"id": "1f00733d-af87-6210-9d66-5714b1916484", "title": "38 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 2400000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "38"}]}, {"id": 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"activo", "value": {"amount": 5100000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "33"}]}, {"id": "1f0072a5-f96c-6f80-9da1-8fea8fb737a4", "title": "18 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 12000000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "18"}]}, {"id": "1f00722a-54a6-6648-bdc6-03414560cb61", "title": "7 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 44352000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "7"}]}, {"id": "1f007368-8390-6334-89ad-b502b56ae14b", "title": "49 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA 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"title": "26 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 560000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "26"}]}, {"id": "1f00730a-792c-6bee-b45c-8d7762ee08d1", "title": "29 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 1632600, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "29"}]}, {"id": "1f00728e-1b8e-65c2-a64d-8fcc83aca1f4", "title": "13 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 7800000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", 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"simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "21"}]}, {"id": "1f007334-5b5f-6fc4-a273-1fae8d73c179", "title": "36 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 1600000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "36"}]}, {"id": "1f007348-e016-6f9c-b3f1-cf75a3d958e9", "title": "40 - 1 - ADQUISICI\u00d3N DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 560000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": false, "attributes": [{"name": "Orden", "value": "1", "id": "40"}]}, {"id": "1f005ab6-9799-621a-8c6e-094885269c05", "title": "1 - 1 - ADQUISICION DE REACTIVOS E INSUMOS PARA LABORATORIO DEL INCAN", "status": "active", "statusDetails": "activo", "value": {"amount": 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