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Medicamentos y Productos Farmaceuticos", "hasEnquiries": false, "value": {"amount": 57442320000, "currency": "PYG"}, "datePublished": "2024-12-20T18:41:25-04:00", "tenderPeriod": {"startDate": "2024-12-20T18:41:25-04:00", "endDate": "2025-05-28T09:00:00-04:00", "durationInDays": 158}, "awardPeriod": {"startDate": "2025-05-28T09:30:00-04:00"}, "contractPeriod": {"maxExtentDate": "2027-12-31T00:00:00-04:00"}, "enquiryPeriod": {"endDate": "2025-05-21T12:00:00-04:00", "startDate": "2024-12-20T18:41:25-04:00", "durationInDays": 151}, "mainProcurementCategory": "services", "additionalProcurementCategories": ["services"], "procurementMethod": "open", "procurementMethodDetails": "Licitaci\u00f3n P\u00fablica Nacional", "procuringEntity": {"id": "DNCP-SICP-CODE-306", "name": "Ministerio de Salud P\u00fablica y Bienestar Social (MSPBS)"}, "criteria": [{"id": "1", "title": "Garant\u00eda de Mantenimiento de Ofertas", "description": "Los oferentes, proveedores o contratistas deber\u00e1n garantizar la seriedad de sus ofertas, mediante la garant\u00eda de mantenimiento de la oferta", "source": "tenderer", "requirementGroups": [{"id": "1-1", "description": "La garant\u00eda debe ser de un cierto porcentaje, periodo y tipo", "requirements": [{"id": "1-1-1", "title": "Porcentaje de la garantia", "expectedValue": "5"}, {"id": "1-1-2", "title": "Validez de la garantia en d\u00edas", "expectedValue": "180"}]}]}], "enquiries": [{"id": "8a948b5a5425ed3db30a72e3b8074164-1", "date": "2025-05-21T11:55:52-04:00", "title": "Capacidad Tecnica", "description": "Se solicita a la convocante aclarar si las documentaciones a ser presentadas y el pais de origen de los documentos, deber\u00e1n emitirse conforme a las agencias indicadas en la Resoluci\u00f3n N\u00ba 148/24 emitida por la DINAVISA", "answer": "Ajustarse al Pliego de Bases y Condiciones.", "dateAnswered": "2025-05-22T11:35:01-04:00"}, {"id": "7611279e5e209a7851181e0134fac1e8-1", "date": "2025-03-24T17:35:43-04:00", "title": "CAPACIDAD TECNICA", "description": "EL PBC CITA CUANTO SIGUE: \u201cPara productos Importados Biol\u00f3gicos: Copia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07. En caso de presentar documentaci\u00f3n emitida por el fabricante con el link web oficial de algunas de las documentaciones citadas anteriormente el mismo debe de estar autenticado por escribano p\u00fablico. Adem\u00e1s del Registro Sanitario emitido por DINAVISA, se debe presentar copia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07. En caso de presentar documentaci\u00f3n emitida por el fabricante con el link web oficial de algunas de las documentaciones citadas anteriormente el mismo debe de estar autenticado por escribano p\u00fablico\u201d\nSolicitamos a la convocante reformular el referido requisito conforme a la reglamentaci\u00f3n vigente seg\u00fan se detalla:\nPara productos Importados Biol\u00f3gicos: Copia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias indicadas seg\u00fan Resoluci\u00f3n N\u00ba 148/24 \u201cpor el cual se emite el listado anual oficial de los pa\u00edses en cumplimiento al Art 3 De la Ley N\u00ba 7256/24\u201d. En caso de presentar documentaci\u00f3n emitida por el fabricante con el link web oficial de algunas de las documentaciones citadas anteriormente el mismo debe de estar autenticado por escribano p\u00fablico. Adem\u00e1s del Registro Sanitario emitido por DINAVISA, se debe presentar copia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias indicadas seg\u00fan Resoluci\u00f3n N\u00ba 148/24 \u201cpor el cual se emite el listado anual oficial de los pa\u00edses en cumplimiento al Art 3 De la Ley N\u00ba 7256/24\u201d. En caso de presentar documentaci\u00f3n emitida por el fabricante con el link web oficial de algunas de las documentaciones citadas anteriormente el mismo debe de estar autenticado por escribano p\u00fablico.\nDicha petici\u00f3n se justifica en consideraci\u00f3n que recientemente (29/05/2024) fue promulgada la Ley 7256/24 \u201cQUE MODIFICA EL ARTICULO 11\u00ba Y AMPLIA LA LEY N\u00ba 3283/2007 \u201cDE PROTECCION DE LA INFORMACION DE LA INFORMACION NO DIVULGADA Y DATOS DE PRUEBA PARA LOS REGISTROS FARMACEUTICOS\u201d, que modific\u00f3 el art\u00edculo 11\u00ba de la ley N\u00ba 3283/2007, el cual traslad\u00f3 a la DINAVISA (art. 3\u00ba de la ley 7256) la responsabilidad de identificar a los citados pa\u00edses en un listado anual oficial siguiendo los criterios y par\u00e1metros establecidos en el art\u00edculo 2\u00ba de la citada normativa y con el fin de no limitar la concurrencia a dicho proceso.", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-04-28T14:26:46-04:00"}, {"id": "d7a84d39cfee0e86eb2c1ff8e485ba2b-1", "date": "2025-01-02T07:47:15-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "A fin de garantizar la calidad y trayectoria del producto a ofertar se sugiere a la entidad convocante ajustar el siguiente requisito de la siguiente manera: \"Para productos importados Biol\u00f3gicos, adem\u00e1s del Registro Sanitario emitido por DINAVISA, se debe presentar copia Legalizada y consularizada y/o apostillada del Registro Sanitario y/o CLV y/o CPP vigente; con antelaci\u00f3n de al menos 3 a\u00f1os, otorgado por alguna de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA y/o agencias regulatorias del MERCOSUR dando cumplimiento a la Ley 7256/2024 y Ley 3283/07.", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-03-07T09:19:50-04:00"}, {"id": "572b9761caa0e4cf8772f37175c7114e-1", "date": "2025-05-21T11:56:03-04:00", "title": "Capacidad T\u00e9cnica", "description": "Para sinteticos y Biologicos, se solicita unificar el criterio en los documentos requeridos: Debiendo ser Registro Sanitario y/o CLV y/o CPP Vigente cualquiera de ellas. o Registro y a parte CLV/CPP ya que ambos documentos acreditan exactamente lo mismo, que es la comercializaci\u00f3n del producto en un pais de alta vigilancia.", "answer": "Ajustarse al Pliego de Bases y Condiciones", "dateAnswered": "2025-05-22T11:35:18-04:00"}, {"id": "ef6078a7b22c7f11a7eb616945f9157d-1", "date": "2024-12-26T10:20:41-04:00", "title": "ABASTECIMIENTO SIMULT\u00c1NEO", "description": "Solicitamos a la convocante modificar el punto ABASTECIMIENTO SIMULTANEO de la siguiente manera:\na. La adjudicaci\u00f3n recaer\u00e1 como m\u00e1ximo en las 3 (tres) mejores ofertas. La adjudicaci\u00f3n se distribuir\u00e1 de la siguiente forma: 50% para la oferta mejor calificada, 30% para la segunda mejor oferta calificada y 20% para la tercera mejor oferta calificada; quienes acepten adecuar su precio al de la oferta evaluada como la m\u00e1s baja.\nb. En caso de que exista 2 (dos) ofertas: La adjudicaci\u00f3n se distribuir\u00e1 de la siguiente forma: 60% para la oferta mejor calificada y 40% para la segunda mejor oferta calificada; quien deber\u00e1 aceptar adecuar su precio al de la oferta evaluada como la m\u00e1s baja.\nc. En caso de que exista 1 (una) sola oferta, y \u00e9sta cumpla con todos los requisitos establecidos en el pliego de bases y condiciones del presente llamado, oferte por la cantidad m\u00e1xima de todos los \u00edtems y tenga la capacidad para ejecutar el contrato, la Convocante podr\u00e1 adjudicar a dicha oferta por la totalidad de lo ofertado.\nEsta solicitud se debe a que al no aplicar el abastecimiento la convocante no solo que restringe la oportunidad a mas potenciales oferentes a ser adjudicados y proveer lo solicitado sino que tambi\u00e9n no existe ning\u00fan criterio t\u00e9cnico que respalde el NO APLICA para este punto.", "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2025-03-07T09:18:12-04:00"}, {"id": "a5e99c9997e2522ed80dc6dffc87cc1e-1", "date": "2025-03-24T11:52:28-04:00", "title": "CAPACIDAD TECNICA", "description": "Con respecto a los requisitos establecidos en la versi\u00f3n 3 publicada en fecha 20/03/25, donde se requiere:\nPara productos Importados Biol\u00f3gicos:\na)\tCopia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nb)\tCopia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07.\nEntendemos que, seleccionar el origen de la emisi\u00f3n de tales documentos a ciertas agencias de alta vigilancia se busca incrementar los controles para asegurar la calidad, seguridad y eficacia del medicamento biol\u00f3gico a ser adquirido m\u00e1s cuando estos, aun no cuentan con antecedentes de uso y de comercializaci\u00f3n en el pa\u00eds.\nEs importante recordar a la convocante que el antecedente de uso de un medicamento en el pa\u00eds es el mayor aseguramiento de que el producto cuenta con las suficientes garant\u00edas de que los beneficios superan en gran manera a los riesgos.\nEs por esta raz\u00f3n que proponemos a la convocante exonerar del cumplimiento de estos requisitos a productos que actualmente vienen siendo comercializados en el mercado nacional y que cuentan con farmacovigilancia activa y sin reportes negativos ante la DINAVISA.\nQue esta exoneraci\u00f3n a mas de otorgar oportunidad a los asiduos proveedores de instituciones de referencia como el MSPBS e IPS tambi\u00e9n podr\u00edan otorgar tales oportunidades a proveedores que cuentan con registro sanitario otorgado por la DINAVISA - primer filtro de control - y que se encuentran comercializando sus productos en el mercado privado o en otras instituciones p\u00fablicas.\nPor lo tanto, dicho esto recomendamos la reformulaci\u00f3n del PBC, de la siguiente manera:\nPara productos Importados Biol\u00f3gicos:\na)\tCopia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nb)\tCopia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07.\nEn caso de presentar documentaci\u00f3n emitida por el fabricante con el link web oficial de algunas de las documentaciones citadas anteriormente el mismo debe de estar autenticado por escribano p\u00fablico.\nEn caso de que los productos ofertados, se encuentren siendo comercializados en el mercado local (biosimilares nacionales o importados), \u00fanicamente deber\u00e1 presentar:\na)\tCopia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nb)\tCopia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nc)\tRegistro sanitario y Certificado de Buenas Pr\u00e1cticas emitido Por la DINAVISA.\nd)\tAntecedentes de uso y comercializaci\u00f3n tales como: contratos de adjudicaci\u00f3n y/o ordenes de compra y/o factura de ventas y/o constancias de uso emitido por los profesionales m\u00e9dicos.", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-04-28T14:26:35-04:00"}, {"id": "f836b6a469b618b9eb078b300c057285-1", "date": "2025-01-02T07:47:33-04:00", "title": "Detalles de bienes y servicios", "description": "Vencimiento: \"El vencimiento m\u00ednimo de los medicamentos no deber\u00e1 ser inferior a 18 (diez y ocho) meses al momento de la entrega..\"\nLa solicitud de una p\u00f3liza por productos con vencimiento de 18 meses solo genera un sobre costo en el producto a ser adquirido por la entidad, se supone que el servicio no estar\u00e1 guardando en sus dep\u00f3sitos productos por m\u00e1s de 12 meses.\nPor lo expuesto, se solicita a la convocante que la obligaci\u00f3n de presentar una p\u00f3liza por el 100% de lo entregado sea modificado solo para productos con 12 meses o menos.", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-03-07T09:20:00-04:00"}, {"id": "429a1f2059256d55d48d747302970934-1", "date": "2025-05-21T11:57:21-04:00", "title": "CAPACIDAD TECNICA", "description": "Cuando dice folletos cat\u00e1logos, se refiere al prospecto que se acompa\u00f1a a la muestra presentada?", "answer": "Ajustarse al Pliego de Bases y Condiciones", "dateAnswered": "2025-05-22T11:35:34-04:00"}, {"id": "99048dca834b862e9090461e993b95c0-1", "date": "2025-01-01T21:11:20-04:00", "title": "ABASTECIMIENTO SIMULTANEO", "description": "A fin asegurar la provisi\u00f3n ininterrumpida de los productos solicitados recomendamos a la convocante aplicar el sistema de abastecimiento simult\u00e1neo a todos los productos solicitados.", "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2025-03-07T09:18:59-04:00"}, {"id": "511d95351d98a245f7a1f710a65966aa-1", "date": "2025-03-24T11:52:19-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "Con respecto a los requisitos establecidos en la versi\u00f3n 3 publicada en fecha 20/03/25, donde se requiere:\nPara productos Importados Biol\u00f3gicos:\na)\tCopia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nb)\tCopia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07.\nEntendemos que, seleccionar el origen de la emisi\u00f3n de tales documentos a ciertas agencias de alta vigilancia se busca incrementar los controles para asegurar la calidad, seguridad y eficacia del medicamento biol\u00f3gico a ser adquirido m\u00e1s cuando estos, aun no cuentan con antecedentes de uso y de comercializaci\u00f3n en el pa\u00eds.\nEs importante recordar a la convocante que el antecedente de uso de un medicamento en el pa\u00eds es el mayor aseguramiento de que el producto cuenta con las suficientes garant\u00edas de que los beneficios superan en gran manera a los riesgos.\nEs por esta raz\u00f3n que proponemos a la convocante exonerar del cumplimiento de estos requisitos a productos que actualmente vienen siendo comercializados en el mercado nacional y que cuentan con farmacovigilancia activa y sin reportes negativos ante la DINAVISA.\nQue esta exoneraci\u00f3n a mas de otorgar oportunidad a los asiduos proveedores de instituciones de referencia como el MSPBS e IPS tambi\u00e9n podr\u00edan otorgar tales oportunidades a proveedores que cuentan con registro sanitario otorgado por la DINAVISA - primer filtro de control - y que se encuentran comercializando sus productos en el mercado privado o en otras instituciones p\u00fablicas.\nPor lo tanto, dicho esto recomendamos la reformulaci\u00f3n del PBC, de la siguiente manera:\nPara productos Importados Biol\u00f3gicos:\na)\tCopia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nb)\tCopia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA tales como FDA, EMA, ANMAT, HEALTH CANADA, ANVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07.\nEn caso de presentar documentaci\u00f3n emitida por el fabricante con el link web oficial de algunas de las documentaciones citadas anteriormente el mismo debe de estar autenticado por escribano p\u00fablico.\nEn caso de que los productos ofertados, se encuentren siendo comercializados en el mercado local (biosimilares nacionales o importados), \u00fanicamente deber\u00e1 presentar:\na)\tCopia Legalizada y consularizada y/o apostillada del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nb)\tCopia Legalizada y consularizada y/o apostillada del Registro Sanitario o CLV o CPP vigente, otorgado por algunas de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA, dando cumplimiento a la Ley 7256/2024 y Ley 3283/07; y;\nc)\tRegistro sanitario y Certificado de Buenas Pr\u00e1cticas emitido Por la DINAVISA.\nd)\tAntecedentes de uso y comercializaci\u00f3n tales como: contratos de adjudicaci\u00f3n y/o ordenes de compra y/o factura de ventas y/o constancias de uso emitido por los profesionales m\u00e9dicos.", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-04-28T14:26:28-04:00"}, {"id": "af1eadb43d4562bb6d40a50baaa87e10-1", "date": "2025-01-02T07:35:49-04:00", "title": "ABASTECIMIENTO SIMULTANEO", "description": "Solicitamos a la Convocante establecer la utilizaci\u00f3n del abastecimiento simultaneo para todos los \u00edtems del proceso. Considerando que el sistema de abastecimiento simultaneo garantiza a la Convocante el abastecimiento de los productos por m\u00e1s de un proveedor, logrando de esta manera una atenci\u00f3n oportuna a los pacientes y otorgando una mayor oportunidad de competencia a todo potencial oferente que cumpla con las condiciones establecidas en el Pliego de Bases y Condiciones para la provisi\u00f3n de todos los productos requeridos.", "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2025-03-07T09:19:10-04:00"}, {"id": "0efc423908202c33b6ee328113f9a2a9-1", "date": "2024-12-23T13:03:49-04:00", "title": "ABASTECIMIENTO SIMULTANEO", "description": "Se solicita a la convocante aplicar el SISTEMA DE ABASTECIMIENTO SIMULTANEO para evitar el desabastecimiento.", "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2025-03-07T09:18:00-04:00"}, {"id": "57d64df17006a11ec21deb11a0bcb708-1", "date": "2025-05-21T11:59:48-04:00", "title": "Vencimiento de los productos", "description": "Se solicita a la convocante reformular dicho apartado solicitando que en caso de entregarse productos con vencimiento menor a 12 meses, all\u00ed reci\u00e9n sea exigencia la presentaci\u00f3n de una p\u00f3liza por fondo de reparo y no para casos con vencimiento de 17 meses para abajo, es importante mencionar que los productos solicitados representan montos de considerable valor econ\u00f3mico.", "answer": "Ajustarse al Pliego de Bases y Condiciones. Los plazos de vencimiento requeridos en el Pliego de Bases y Condiciones fueron establecidos conforme a las necesidades del Programa. ", "dateAnswered": "2025-05-22T11:35:59-04:00"}, {"id": "09b7a73a5eed0ff9eb3cf81d4aad2b8d-1", "date": "2025-01-01T21:11:06-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "Se sugiere a la convocante agregar el siguiente requisito: \"Para productos importados Biol\u00f3gicos, no deben tener rechazo de autorizaci\u00f3n de comercializaci\u00f3n en ninguna de las Agencias regulatorias previstas en la lista anual oficial de los pa\u00edses emitida por DINAVISA y/o agencias regulatorias del MERCOSUR dando cumplimiento a la Ley 7256/2024 y Ley 3283/07.", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-03-07T09:18:48-04:00"}, {"id": "1b9f3d61ef86005619df28163e502149-1", "date": "2025-01-01T21:11:00-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "Para garantizar la calidad del producto a adquirir, recomendamos a la entidad convocante incluir el siguiente requisito: 'Los productos biol\u00f3gicos, ya sean innovadores o biosimilares, deber\u00e1n contar con un registro sanitario vigente emitido por la Direcci\u00f3n Nacional de Vigilancia Sanitaria (DINAVISA), con una anticipaci\u00f3n m\u00ednima de dos a\u00f1os.'", "answer": "Ajustarse al PBC.-", "dateAnswered": "2025-03-07T09:18:36-04:00"}, {"id": "dd26e13f53fa4c20feb1c750702e6355-1", "date": "2025-01-02T07:42:03-04:00", "title": "Experiencia requerida", "description": "En cuanto a la experiencia requerida, solicitamos considerar la experiencia adquirida en el 2024, ya que corresponde a un a\u00f1o cerrado y no existe impedimento para validar la experiencia adquirida en dicho periodo.", "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2025-03-07T09:19:30-04:00"}], "lots": [{"id": "1efb8b3d-fa83-6a30-bd7b-fb20e456cc4e", "title": "1 - 1 - Rituximab inyectable", "status": "active", "statusDetails": "activo", "value": {"amount": 55432080000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "1", "id": "1"}]}, {"id": "1efb8b3f-ee02-64c6-9642-c1738de6d4f4", "title": "2 - 2 - Leflunomida comprimido", "status": "active", "statusDetails": "activo", "value": {"amount": 2010240000, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "2", "id": "2"}]}], "items": [{"id": "1efb8b3f-ee06-66fc-9d58-c1738de6d4f4", "description": "Leflunomida comprimido", "classification": {"scheme": "catalogoNivel5DNCP", "id": "51142130-001", "description": "Leflunomida comprimido", "uri": "https://www.contrataciones.gov.py/datos/api/v3/doc/itemClassification/n5/51142130-001"}, "additionalClassifications": [{"scheme": "UNSPSC", "id": "51142130", "description": "Leflunomida", "uri": "https://www.contrataciones.gov.py/datos/api/v3/doc/itemClassification/n4/51142130"}], "quantity": 480000, "minQuantity": 240000, "unit": {"name": "Unidad", "id": "UNI", "value": {"amount": 4188, "currency": "PYG"}}, "relatedLot": "1efb8b3f-ee02-64c6-9642-c1738de6d4f4", "attributes": [{"name": "Presentacion", "value": "UNIDAD", "id": "1"}, {"name": "Orden", "value": "2", "id": "2"}]}, {"id": "1efb8b3d-fa8c-6c20-8015-fb20e456cc4e", "description": "Rituximab inyectable", "classification": {"scheme": "catalogoNivel5DNCP", "id": "51111716-001", "description": "Rituximab inyectable", "uri": "https://www.contrataciones.gov.py/datos/api/v3/doc/itemClassification/n5/51111716-001"}, "additionalClassifications": [{"scheme": "UNSPSC", "id": "51111716", "description": "Rituximab", "uri": "https://www.contrataciones.gov.py/datos/api/v3/doc/itemClassification/n4/51111716"}], "quantity": 4800, "minQuantity": 2400, "unit": {"name": "Unidad", "id": "UNI", "value": {"amount": 11548350, "currency": "PYG"}}, "relatedLot": "1efb8b3d-fa83-6a30-bd7b-fb20e456cc4e", "attributes": [{"name": "Presentacion", "value": "VIAL", "id": "1"}, {"name": "Orden", "value": "1", "id": "2"}]}], "tenderers": [{"name": "TARGET S.A", "id": "PY-RUC-80025423-6"}, {"name": "DISTRIBUIDORA LA POLICLINICA S. 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