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En tal sentido, se comunica que la convocante mantiene lo establecido en el PBC.", "dateAnswered": "2025-10-01T13:17:36-04:00"}, {"id": "44e98ec6b5ad3c46df320948c7ab0b8c-1", "date": "2025-09-26T16:40:47-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "En el punto 3 la convocante solicita la presentaci\u00f3n del Registro Sanitario expedido por la DINAVISA, para los medicamentos.\nAl respecto solicitamos tambi\u00e9n sea un requerimiento la presentaci\u00f3n del registro sanitario vigente expedido por la DINAVISA a nombre del oferente para dispositivos m\u00e9dicos, y no solo para medicamentos.", "answer": "En atenci\u00f3n a la solicitud presentada, se informa que el requerimiento establecido en el Pliego de Bases y Condiciones fue definido conforme a las necesidades identificadas para el presente proceso, por lo que el mismo se ajusta plenamente. En tal sentido, se comunica que la convocante mantiene lo establecido en el PBC.", "dateAnswered": "2025-10-01T13:17:52-04:00"}, {"id": "0a4fb778c556a61d8faaf6c530836182-1", "date": "2025-09-24T12:28:01-04:00", "title": "Capacidad t\u00e9cnica", "description": "Solicitamos incluir para Dispositivos m\u00e9dicos los siguientes requisitos:\nPara Importadores, Representantes de Dispositivos m\u00e9dicos importados:\n\u2022\tCopia autenticada de la correspondiente resoluci\u00f3n de apertura vigente que lo habilite para importar y/o comercializar dispositivos medicos, seg\u00fan sea el caso.\n\u2022\tCertificado de buenas pr\u00e1cticas de almacenamientos (deposito).\n\u2022\tCertificado de registro sanitario vigente del producto ofertado", "answer": "En relaci\u00f3n a la consulta formulada, se le informa que los requisitos mencionados ya se encuentran previstos en el Pliego de Bases y Condiciones, espec\u00edficamente en el punto 6. Por lo tanto, se solicita remitirse al mismo. ", "dateAnswered": "2025-10-01T13:17:47-04:00"}, {"id": "60322be6bc04473bc344bca3ce6b2e1d-1", "date": "2025-09-24T15:06:53-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "En el punto donde se solicita lo siguiente:\nDocumentaci\u00f3n expedida por el Fabricante que los acredite como representante de la marca ofertada y centro autorizado de servicios (CAS), soporte y servicio de posventa, dichos documentos deben estar debidamente legalizados por el Consulado Paraguayo del Pa\u00eds de emisi\u00f3n del documento y del Ministerio de Relaciones Exteriores de la Rep\u00fablica del Paraguay. Los mismos deben ser originales o copias autenticadas por Escribano P\u00fablico.\nAl respecto solicitamos que en este criterio sea requerido de la siguiente manera:\nDocumentaci\u00f3n expedida por el Fabricante que los acredite como representante de la marca ofertada y centro autorizado de servicios (CAS), soporte y servicio de posventa, dichos documentos deben estar debidamente legalizados por el Consulado Paraguayo y/o apostillado en el Pa\u00eds de emisi\u00f3n del documento y del Ministerio de Relaciones Exteriores de la Rep\u00fablica del Paraguay. Los mismos deben ser originales o copias autenticadas por Escribano P\u00fablico.", "answer": "Con relaci\u00f3n a su consulta, se aclara que el requerimiento de autorizaci\u00f3n del fabricante responde a lo necesario para el proceso, por lo que la Instituci\u00f3n mantiene lo establecido, sin modificaciones.", "dateAnswered": "2025-10-01T13:17:50-04:00"}, {"id": "b376ee9dfc7e0e13c8b88b4890a4541b-1", "date": "2025-09-24T12:27:40-04:00", "title": "Requisitos documentales para evaluar el criterio de capacidad t\u00e9cnica", "description": "En el punto 3 la convocante solicita lo siguiente:\nContar con Registro Sanitario expedido por la DINAVISA, para los medicamentos.\nAl respecto solicitamos que en este requisito se modifique e incluya la solicitud del registro sanitario vigente expedido por la DINAVISA para dispositivos m\u00e9dicos y quede establecido de la Sgte. manera:,\nContar con Registro Sanitario vigente expedido por la DINAVISA, para los medicamentos y dispositivos m\u00e9dicos, teniendo en cuenta que el llamado no solo contempla adquisici\u00f3n de medicamentos.", "answer": "En atenci\u00f3n a la solicitud presentada, se informa que el requerimiento establecido en el Pliego de Bases y Condiciones fue definido conforme a las necesidades identificadas para el presente proceso, por lo que el mismo se ajusta plenamente. En tal sentido, se comunica que la convocante mantiene lo establecido en el PBC.", "dateAnswered": "2025-10-01T13:17:38-04:00"}, {"id": "1d406e2f97df8794f2922f9a0a5f02d9-1", "date": "2025-09-24T12:27:14-04:00", "title": "Capacidad t\u00e9cnica", "description": "En el punto 3 la convocante solicita lo siguiente:\nContar con Registro Sanitario expedido por la DINAVISA, para los medicamentos.\nAl respecto solicitamos que en este requisito se modifique e incluya el registro sanitario vigente expedido por la DINAVISA para dispositivos m\u00e9dicos y quede establecido de la Sgte. manera:,\nContar con Registro Sanitario vigente expedido por la DINAVISA, para los medicamentos y dispositivos m\u00e9dicos, teniendo en cuenta que el llamado no solo contempla adquisici\u00f3n de medicamentos.", "answer": "En atenci\u00f3n a la solicitud presentada, se informa que el requerimiento establecido en el Pliego de Bases y Condiciones fue definido conforme a las necesidades identificadas para el presente proceso, por lo que el mismo se ajusta plenamente. 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