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DINAVISA N\u00b0 148/2024, es m\u00e1s que suficiente para dar por cumplido con el requisito, ya que entendemos que la convocante busca asegurar que los productos ofertados importados cumplen con las garant\u00edas de calidad, seguridad y eficacia.", "answer": "Remitirse a la \u00faltima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T14:47:37-04:00"}, {"id": "6ddefdc506c3e8aca2c97a78798439e7-1", "date": "2025-10-21T11:12:56-04:00", "title": "EXPERIENCIA REQUERIDA", "description": "Con el objetivo de calificar la experiencia del oferente, se considerar\u00e1n los siguientes \u00edndices: Demostrar la experiencia en MEDICAMENTOS con facturaciones de venta y/o contratos con sus respectivas actas de recepci\u00f3n y/o nota de remisi\u00f3n, tanto en el sector p\u00fablico como en el sector privado, por un monto equivalente al [25] % como m\u00ednimo del monto m\u00e1ximo ofertado en la presente licitaci\u00f3n, de los: 3 (tres) \u00faltimos a\u00f1os, 2022 2023-2024. Con relaci\u00f3n a los contratos con sus respectivas actas de recepci\u00f3n y/o nota de remisi\u00f3n, solicitamos a la convocante excluir la presentaci\u00f3n ACTAS Y/O NOTAS DE REMISION atendiendo al monto del llamado y este podr\u00eda resultar una limitante para potenciales oferentes, adem\u00e1s con la presentaci\u00f3n de facturas y/o contratos la convocante ya asegura el cumplimiento del oferente en dicho requisito.", "answer": "La Convocante requiere la experiencia demostrada con la ejecuci\u00f3n de contratos o el nivel de facturaci\u00f3n con el documento de resguardo de la entrega efectiva del producto demostrado a trav\u00e9s de o actas de recepci\u00f3n y/o nota de remisi\u00f3n, tanto en el sector p\u00fablico y/o privado. El periodo de a\u00f1os y la habilitaci\u00f3n de documentos de provisi\u00f3n tanto en el sector p\u00fablico como en el privado habilita a potenciales oferentes que cumplan con los requisitos de participaci\u00f3n.", "dateAnswered": "2025-11-04T14:49:33-04:00"}, {"id": "5485a5654bc555ea4093aa46d2db8e69-1", "date": "2025-10-21T11:35:47-04:00", "title": "Experiencia requerida", "description": "La entidad indica: MEDICAMENTOS con facturaciones de venta y/o contratos con sus respectivas actas de recepci\u00f3n y/o nota de remisi\u00f3n.. No queda claro si se debe presentar FACTURAS+REMISION o, CONTRATOS + REMISION. La redacci\u00f3n genera demasiadas ambig\u00fcedades que complican a la hora de ofertar y podr\u00edan desembocar en  adjudicaciones arbitrarias. Solicitamos a la convoncante delimitar y establecer correctamente los documentos a ser evaluados.", "answer": "La redacci\u00f3n permite la presentaci\u00f3n de facturas con sus respectivas actas de recepci\u00f3n y/o notas de remisi\u00f3n,  as\u00ed como contratos con sus respectivas actas de recepci\u00f3n y/o notas de remisi\u00f3n,  determinando la conjunci\u00f3n \"y\"  la posibilidad de presentar tanto contratos como facturas  con sus respectivas actas de recepci\u00f3n y nota de remisi\u00f3n. El oferente puede optar por acompa\u00f1ar unicamente de actas de recepci\u00f3n o unicamente por notas de remisi\u00f3n cada contrato o facturaci\u00f3n.", "dateAnswered": "2025-10-23T16:28:41-04:00"}, {"id": "73220e9b9e50e712f1a449b9a5797c3b-1", "date": "2025-10-29T11:43:06-04:00", "title": "Plan de Entrega de los bienes", "description": "Se sugiera a la convocante excluir el plazo de emisi\u00f3n de la primera orden (dentro de los 20 d\u00edas corridos) a fin de que la entidad pueda manejar sus emisiones de a cuerdo la necesidad real de los pacientes.", "answer": "El periodo que estipula la Convocante permite administrar las necesidades reales del INCAN y Centros de la Red Oncol\u00f3gica.", "dateAnswered": "2025-11-04T15:26:37-04:00"}, {"id": "478402bd5dd8848dc11062764b118c3c-1", "date": "2025-10-21T11:49:29-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "Se solicita incorporar como requisito documental la presentaci\u00f3n de una Constancia o Certificaci\u00f3n de Buenas Pr\u00e1cticas de Farmacovigilancia vigente, emitida por la Direcci\u00f3n Nacional de Vigilancia Sanitaria (DINAVISA), aplicable a todo OFERENTE, sea nacional o importado.\nConforme a la Ley N\u00b0 1119/97, la Ley N\u00b0 3283/07 y su modificaci\u00f3n por la Ley N\u00b0 7256/24, as\u00ed como la Resoluci\u00f3n DINAVISA N\u00b0 51/2022, la responsabilidad sobre la farmacovigilancia y el seguimiento post-comercializaci\u00f3n recae en el titular del registro sanitario o su representante local. Por tanto, corresponde exigir la constancia de cumplimiento de Buenas Pr\u00e1cticas de Farmacovigilancia como condici\u00f3n t\u00e9cnica para garantizar la seguridad y trazabilidad de los productos ofertados.", "answer": "Remitirse a la \u00faltima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T15:03:28-04:00"}, {"id": "6facf457b09f491c53f392b606732b08-1", "date": "2025-10-29T11:27:07-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "La convocante dice: Cuando el pa\u00eds de origen del elaborador no es clasificado conforme al Art. 1 de la LEY N\u00b0 7256/24 QUE MODIFICA EL ARTICULO 11\u00b0 Y AMPLIA LA LEY N\u00b0 3283/2007 y RES. DINAVISA N\u00b0148/24 POR LA CUAL SE EMITE EL LISTADO ANUAL OFICIAL DE LOS PAISES EN CUMPLIMIENTO AL ART.3 DE LA LEY N\u00b0 7256/24 o no forme parte del MERCOSUR, deber\u00e1 presentar Certificado de Buenas Practicas de Fabricaci\u00f3n vigente emitido por la Agencia Reguladora de medicamentos del pa\u00eds de origen o Licencia/Certificado de Fabricaci\u00f3n vigente del producto ofertado. Adem\u00e1s, deber\u00e1 presentar el certificado de Buenas Practicas de fabricaci\u00f3n del fabricante vigente o 21/41 Licencia/Certificado de Fabricaci\u00f3n vigente emitido por cualquiera de las agencias declaradas en la LEY N\u00b0 7256/24 y RES. DINAVISA N\u00b0 148/24 o el REGISTRO SANITARIO del producto ofertado emitido por cualquiera de las agencias declaradas en la Ley N\u00b07256/24. -  Consulta: se podr\u00eda presentar CPP/CLV en reemplazo del REGISTRO SANITARIO emitido por las agencias declaradas en la Ley N\u00b0 7256/24. de ser as\u00ed, favor modificar el pliego permitiendo dicho requisito.", "answer": "El Registro Sanitario emitido por cualquiera de las agencias declaradas en la Ley N\u00b0 7256/24 es una alternativa conforme la redacci\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T15:44:02-04:00"}, {"id": "e94938a5e9f2dd9537f32f60df57af1a-1", "date": "2025-10-21T11:28:00-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "Se recomienda a la convocante incluir la presentaci\u00f3n de protocolos da FARMACOVIGILANCIA atendiendo la complejidad y naturaleza de los productos a ser adquiridos.", "answer": "Se requieren las Buenas Pr\u00e1cticas de Farmacovigilancia emitida por la Direcci\u00f3n Nacional de Vigilancia Sanitaria. Remitirse a la ultima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T14:53:55-04:00"}, {"id": "6bca84d3bea2a7e03a899a3a11057f55-1", "date": "2025-10-27T17:51:12-04:00", "title": "CAPACIDAD TECNICA", "description": "Solicitamos a la convocante a incluir para los casos de productos importados LINK WEB oficial donde se puede acreditar que el fabricante cuenta con Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente o Certificado de Registro sanitario vigente en alguno de los pa\u00edses indicados como de alta vigilancia conforme al Art. 1 de la LEY N\u00b0 7256/24 y RES. DINAVISA N\u00b0 148/2024, es m\u00e1s que suficiente para dar por cumplido con el requisito, ya que entendemos que la convocante busca asegurar que los productos ofertados importados cumplen con las garant\u00edas de calidad, seguridad y eficacia.", "answer": "Remitirse a la ultima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T15:29:23-04:00"}, {"id": "682b7ae5ab9b35744a1ac0c1c7f2a16f-1", "date": "2025-10-29T10:41:05-04:00", "title": "Documentos que avalan experiencia", "description": "Se solicita unificar criterios entre lo expuesto en \"Experiencia requerida\" y \"Requisitos documentales para la evaluaci\u00f3n de la experiencia\", la falta de criterios unificados genera inconvenientes a la hora de presentar los documentos correctos e incluso generar\u00e1 inconvenientes al momento de evaluar.", "answer": "Remitirse a la ultima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T15:55:25-04:00"}, {"id": "635e982163b144095609c302f26f3ed2-1", "date": "2025-10-21T11:23:53-04:00", "title": "Experiencia requerida - Requisitos documentales", "description": "Se solicita unificar los documentos requeridos. En experiencia solicitan:  \"facturaciones de venta y/o contratos con sus respectivas actas de recepci\u00f3n y/o nota de remisi\u00f3n\" y en Requisitos documentales: \"Copia de Facturas y/o contratos con sus respectivas recepciones finales\"", "answer": "Remitirse a la ultima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T15:55:21-04:00"}, {"id": "3bb8217141712e5cbb4d9fc7b1a95340-1", "date": "2025-10-29T11:25:42-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "La convocante no est\u00e1 solicitando aplicar estrategias de farmacovigilancias a trav\u00e9s de planes de gesti\u00f3n de riesgos o vigilancias activas. Con el prop\u00f3sito realizar un seguimiento a la eficacia de los productos que el INCAN est\u00e1 adquiriendo, recomendamos incluir entre sus requisitos la presentaci\u00f3n de documentos con \"Planes de gesti\u00f3n de riesgos\" o protocolos de Farmacovigilancia Activa.", "answer": "Se contempla el requisito de Buenas Practicas de Farmacovigilancia emitida por la Direcci\u00f3n Nacional de Vigilancia Sanitaria. Remitirse al pliego de Bases y Condiciones.", "dateAnswered": "2025-11-04T15:54:37-04:00"}, {"id": "a4fe513f75b16a8d6badf0f3253451f5-1", "date": "2025-10-17T16:34:14-04:00", "title": "CAPACIDAD TECNICA- INCISO 5. BUENAS PRACTICAS", "description": "Solicitamos a la convocante a incluir para los casos de productos importados LINK WEB oficial donde se puede acreditar que el fabricante cuenta con Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente o Certificado de Registro sanitario vigente en alguno de los pa\u00edses indicados como de alta vigilancia conforme al Art. 1 de la LEY N\u00b0 7256/24 y RES. DINAVISA N\u00b0 148/2024, es m\u00e1s que suficiente para dar por cumplido con el requisito, ya que entendemos que la convocante busca asegurar que los productos ofertados importados cumplen con las garant\u00edas de calidad, seguridad y eficacia.", "answer": "Remitirse a la \u00faltima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T14:47:30-04:00"}, {"id": "dff644ebe7b8796abab27bb561cacee4-1", "date": "2025-10-21T11:49:18-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "Para productos importados: copia autenticada del Certificado de Buenas Pr\u00e1cticas de Almacenamiento emitido a nombre del\nOFERENTE. Se solicita que, en caso de que el oferente no sea titular del registro sanitario, la presentaci\u00f3n del Certificado de Buenas Pr\u00e1cticas sea tanto del OFERENTE, TITULAR/REPRESENTANTE EN EL PAIS y el FABRICANTE. Esto asegura la cadena de Buenas pr\u00e1cticas del producto a ser adquirido.", "answer": "Los requisitos de Buenas Pr\u00e1cticas de Fabricaci\u00f3n, Control y/o Almacenamiento se estipulan claramente en el Pliego de Bases y Condiciones.", "dateAnswered": "2025-11-04T15:03:02-04:00"}, {"id": "b58bf3695612e2dc46825fbbe9cb7400-1", "date": "2025-10-17T16:34:03-04:00", "title": "EXPERIENCIA REQUERIDA- DECLARACION JURADA", "description": "En el PBC se establece como requisito la presentaci\u00f3n de lo sgte: Para el caso de MEDICAMENTOS IMPORTADOS y que el oferente no sea el fabricante y/o el titular del registro sanitario de los medicamentos, dicha experiencia deber\u00e1 estar igualmente acreditada por el oferente, por el titular del registro sanitario y el fabricante del producto que se oferta. La experiencia del fabricante extranjero podr\u00e1 ser igualmente acreditada con una declaraci\u00f3n jurada en la cual se indique claramente que cumple con el porcentaje requerido. \nObservaci\u00f3n \nLa redacci\u00f3n actual no precisa con claridad qui\u00e9n debe emitir dicha declaraci\u00f3n, generando dudas sobre si corresponde al titular del Registro Sanitario o directamente al fabricante extranjero. \nPropuesta de Aclaraci\u00f3n \nSolicitamos se confirme que: \n\u2022 La Declaraci\u00f3n Jurada de experiencia debe ser emitida por el fabricante extranjero, en cuanto es responsable directo de la producci\u00f3n y poseedor de la informaci\u00f3n sobre su trayectoria t\u00e9cnica e industrial. \n\u2022 En los casos en que el titular del Registro Sanitario no coincida con el fabricante, este podr\u00e1 acompa\u00f1ar o ratificar la declaraci\u00f3n, a fin de asegurar trazabilidad y coherencia legal en la documentaci\u00f3n presentada. Fundamentaci\u00f3n \n\u2022 La exigencia recae sobre la capacidad productiva del fabricante, lo que hace indispensable que sea \u00e9l quien emita la declaraci\u00f3n. \n\u2022 Permitir que el titular del Registro Sanitario ratifique o acompa\u00f1e la misma aporta seguridad jur\u00eddica y evita vac\u00edos formales, sin desvirtuar el objetivo del requisito. \n\u2022 De este modo se garantiza transparencia, coherencia documental y se respeta el principio de legalidad en los procesos de adquisici\u00f3n p\u00fablica.", "answer": "Remitirse a la \u00faltima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T14:46:57-04:00"}, {"id": "5097b1e3b3fbc4f6f8fd3793968f1df0-1", "date": "2025-10-10T15:58:48-04:00", "title": "Especificaciones t\u00e9cnicas", "description": "Se solicita a la convocante especificar la forma farmac\u00e9utica en el apartado de especificaciones t\u00e9cnicas. PARA CADA ITEM", "answer": "Se han realizado modificaciones en el Pliego de Bases y Condiciones. Remitirse a la \u00faltima versi\u00f3n del Pliego de Bases y Condiciones.", "dateAnswered": "2025-10-23T15:59:54-04:00"}, {"id": "04af556d6e68ee6328e7bf31a834cf4e-1", "date": "2025-10-29T11:43:15-04:00", "title": "Plan de Entrega de los bienes", "description": "En el PBC se establece: Las \u00f3rdenes de\ncompras seran emitidas una vez emitida la totalidad de las cantidades m\u00ednimas, donde se deber\u00e1 emitir hasta 30 d\u00edas antes de la fecha\nde tope de vigencia del contrato, con un plazo de entrega de hasta 15(quince) d\u00edas corridos contados a partir de la recepci\u00f3n de las\nordenes de compra emitida. Recomendamos a la convocante excluir este procedimiento de tener que emitir las ordenes como m\u00e1ximo antes de los 30 d\u00edas de finalizaci\u00f3n del contrato, con la particularidad de que el plazo de entrega cambia a 15(quince) d\u00edas corridos. Esta instrucci\u00f3n genera, adem\u00e1s de confusiones innecesarias, una restricci\u00f3n de emitir dentro del plazo (hasta el vencimiento del contrato) las ordenes de compras en base a necesidad de la entidad. Es como ir en contra de los intereses del paciente.", "answer": "La estipulaci\u00f3n del procedimiento es a efectos de otorgar seguridad jur\u00eddica a las Partes, en el marco de la vigencia del contrato y las garant\u00edas contractuales.", "dateAnswered": "2025-11-04T15:28:59-04:00"}, {"id": "f96e1ff8f0106173051042db4f50dd9d-1", "date": "2025-10-29T11:27:02-04:00", "title": "Presentaci\u00f3n Item 3", "description": "Solicitamos a la convocante ampliar la presentaci\u00f3n del Item 3 a: Comprimidos/tabletas recubiertas/c\u00e1psulas. Lo solicitado solo limita la participaci\u00f3n a potenciales oferentes.", "answer": "La Convocante requiere la presentaci\u00f3n en comprimidos conforme los antecedentes de la programaci\u00f3n de la compra, permitiendo la participaci\u00f3n a los potenciales oferentes que califiquen legal, t\u00e9cnica y econ\u00f3micamente.  ", "dateAnswered": "2025-11-04T15:46:47-04:00"}, {"id": "ff9ee0bf3e9052f3f6d28fc7f86bfaa7-1", "date": "2025-10-29T11:26:57-04:00", "title": "Precio refencial Item 3", "description": "Se solicita a la convocante analizar el precio referencial establecido. El mismo se encuentra muy por debajo del precio de mercado actual.", "answer": "El precio referencial fue determinado 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 limitativo. ", "dateAnswered": "2025-11-04T15:32:38-04:00"}, {"id": "04e779042b59cf10e6f997b8db87fbeb-1", "date": "2025-10-29T09:25:29-04:00", "title": "Capacidad Tecnica", "description": "Para productos importados: copia autenticada del Certificado de Buenas Pr\u00e1cticas de Almacenamiento emitido a nombre del OFERENTE expedido por la Direcci\u00f3n Nacional de Vigilancia Sanitaria (DINAVISA).\nCuando el pa\u00eds de origen del elaborador es clasificado conforme al Art. 1 de la LEY N\u00b0 7256/24 QUE MODIFICA EL ARTICULO 11\u00b0 Y AMPLIA LA LEY N\u00b03283/2007 DE PROTECCION DE LA INFORMACION NO DIVULGADA Y DATOS DE PRUEBA PARA LOS REGISTROS FARMACEUTICOS y RES. DINAVISA N\u00b0 148/2024 POR LA CUAL SE EMITE EL LISTADO ANUAL OFICIAL DE LOS PAISES EN CUMPLIMIENTO AL ART. 3 DE LA LEY N\u00b07256/24, deber\u00e1 presentar el Certificado de Buenas Practicas de Fabricaci\u00f3n vigente o Licencia/Certificado de Fabricaci\u00f3n del producto ofertado o formar parte del MERCOSUR.\nCuando el pa\u00eds de origen del elaborador no es clasificado conforme al Art. 1 de la LEY N\u00b0 7256/24 QUE MODIFICA EL ARTICULO 11\u00b0 Y AMPLIA LA LEY N\u00b0 3283/2007 y RES. DINAVISA N\u00b0148/24 POR LA CUAL SE EMITE EL LISTADO ANUAL OFICIAL DE LOS PAISES EN CUMPLIMIENTO AL ART.3 DE LA LEY N\u00b0 7256/24 o no forme parte del MERCOSUR, deber\u00e1 presentar Certificado de Buenas Practicas de Fabricaci\u00f3n vigente emitido por la Agencia Reguladora de medicamentos del pa\u00eds de origen o Licencia/Certificado de Fabricaci\u00f3n vigente del producto ofertado. Adem\u00e1s, deber\u00e1 presentar el certificado de Buenas Practicas de fabricaci\u00f3n del fabricante vigente o Licencia/Certificado de Fabricaci\u00f3n vigente emitido por cualquiera de las agencias declaradas en la LEY N\u00b0 7256/24 y RES. DINAVISA N\u00b0 148/24 o el Registro Sanitario del producto ofertado emitido por cualquiera de las agencias declaradas en la Ley N\u00b07256/24\n\nSolicitamos  a la convocante reformular de la siguiente manera: \nPara productos importados: copia autenticada del Certificado de Buenas Pr\u00e1cticas de Almacenamiento emitido a nombre del OFERENTE expedido por la Direcci\u00f3n Nacional de Vigilancia Sanitaria (DINAVISA).\nCuando el pa\u00eds de origen del elaborador es clasificado conforme al Art. 1 de la LEY N\u00b0 7256/24 QUE MODIFICA EL ARTICULO 11\u00b0 Y AMPLIA LA LEY N\u00b03283/2007 DE PROTECCION DE LA INFORMACION NO DIVULGADA Y DATOS DE PRUEBA PARA LOS REGISTROS FARMACEUTICOS y RES. DINAVISA N\u00b0 148/2024 POR LA CUAL SE EMITE EL LISTADO ANUAL OFICIAL DE LOS PAISES EN CUMPLIMIENTO AL ART. 3 DE LA LEY N\u00b07256/24, deber\u00e1 presentar el Certificado de Buenas Practicas de Fabricaci\u00f3n vigente o Licencia/Certificado de Fabricaci\u00f3n del producto ofertado o formar parte del MERCOSUR.\nCuando el pa\u00eds de origen del elaborador no es clasificado conforme al Art. 1 de la LEY N\u00b0 7256/24 QUE MODIFICA EL ARTICULO 11\u00b0 Y AMPLIA LA LEY N\u00b0 3283/2007 y RES. DINAVISA N\u00b0148/24 POR LA CUAL SE EMITE EL LISTADO ANUAL OFICIAL DE LOS PAISES EN CUMPLIMIENTO AL ART.3 DE LA LEY N\u00b0 7256/24 o no forme parte del MERCOSUR, deber\u00e1 presentar Certificado de Buenas Practicas de Fabricaci\u00f3n vigente emitido por la Agencia Reguladora de medicamentos del pa\u00eds de origen o Licencia/Certificado de Fabricaci\u00f3n vigente del producto ofertado. Adem\u00e1s, deber\u00e1 presentar el certificado de Buenas Practicas de fabricaci\u00f3n del fabricante vigente o Licencia/Certificado de Fabricaci\u00f3n vigente emitido por cualquiera de las agencias declaradas en la LEY N\u00b0 7256/24 y RES. DINAVISA N\u00b0 148/24 o el Registro Sanitario del producto ofertado emitido por cualquiera de las agencias declaradas en la Ley N\u00b07256/24\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", "answer": "Remitirse a la ultima versi\u00f3n del pliego de bases y condiciones.", "dateAnswered": "2025-11-04T15:29:31-04:00"}, {"id": "7156a6967f6a7c210f987fa2b850cc79-1", "date": "2025-10-29T10:43:25-04:00", "title": "Experiencia requerida", "description": "La convocante expresa: Demostrar la experiencia en MEDICAMENTOS con facturaciones de venta y/o contratos con sus respectivas actas de recepci\u00f3n y/o NOTA DE REMISION. Es necesario recordar que las Notas de remisi\u00f3n no contemplan montos, solo cantidades, en consecuencia la sola presentaci\u00f3n de NOTA DE REMISION no ser\u00e1 un documento analizable para determinar el cumplimiento de este requisito. Se sugiere a la convocante excluir las NOTA DE REMISION como documento posible a presentar.", "answer": "Con la factura se podr\u00e1 contabilizar el monto y con la nota de remisi\u00f3n se certificar\u00e1 la entrega/recepci\u00f3n efectiva , lo cual es el objetivo de la calificaci\u00f3n en experiencia requerida.", "dateAnswered": "2025-11-04T15:31:54-04:00"}], "lots": [{"id": "1f09ebfa-3d89-6c50-9ebb-b9835854c2f2", "title": "2 - 2 - Abiraterona Acetato Comprimido", "status": "active", "statusDetails": "activo", "value": {"amount": 110246387472, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "2", "id": "2"}]}, {"id": "1f09ebfc-bce7-6770-a0d1-b72fa9c60ef3", "title": "3 - 3 - Capecitabina comprimido", "status": "active", "statusDetails": "activo", "value": {"amount": 5574759288, "currency": "PYG"}, "openContractType": "cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "3", "id": 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