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SE ACLARA AL OFERENTE QUE DEBER\u00c1 PRESENTAR EL SIGUIENTE DOCUMENTO: \n3. El oferente deber\u00e1 presentar copia del Certificado de Registro Sanitario Vigente, emitido por la Direcci\u00f3n Nacional de Vigilancia Sanitaria.", "dateAnswered": "2022-10-04T10:14:19-04:00"}, {"id": "fd2def4cf6bf414c7442b600c7cce8fb", "date": "2022-09-28T18:05:08-04:00", "title": "requisito para evaluar capacidad tecnica", "description": "Para el punto 17. Estudio de Bioequivalencia comparable con el producto de referencia, a fin de garantizar la calidad, eficiencia y efectividad de los productos\nSolicitamos a la convocante consideracion y para los productos de origen nacional, que sea suficiente aval la presentacion del registro sanitario emitida por la DNVS, en vista de que dicho documento no forma parte del requerimiento solicitado por la agencia reguladora para el registro del producto, por lo que dicho requerimiento, limita imnecesariamente la participacion productos de origen nacional", "answer": "REMITIRSE A LA ADENDA N\u00b0 1 - PBC VERSI\u00d3N 2. SE ACLARA AL OFERENTE QUE DICHO REQUISITO FUE EXCLUIDO DEL PBC.", "dateAnswered": "2022-10-04T10:14:22-04:00"}, {"id": "da359a94ace0bd406eb8b105d21b9017", "date": "2022-09-28T18:19:39-04:00", "title": "especificaciones tecnica", "description": "la convocante solicita en Nombre del producto: Tacrolimus capsula, concentracion 0,5 mg capsulas duras no obstante en forma farmaceutica solicita comprimido, lo ultimo expuesto contradice los requerimientos de capsulas declarada en el nombre del producto y en la concentracion, por lo que consultamos si, la forma farmaceutica que la convocante desea solicitar es en capsulas duras, asi mismo tambien aclaramos que la forma farmaceutica en comprimidos a la fecha no se encuentra disponible en el mercado", "answer": "REMITIRSE A LA ADENDA N\u00b0 1 - PBC VERSI\u00d3N 2. SE ACLARA AL OFERENTE QUE LA FORMA FARMAC\u00c9UTICA REQUERIDA SER\u00c1: C\u00c1PSULAS.", "dateAnswered": "2022-10-04T10:14:34-04:00"}, {"id": "92523c5ad9f62de329f7cfaa87ac860f", "date": "2022-09-28T18:14:05-04:00", "title": "requisito para evaluar capacidad tecnica", "description": "para el punto 17 Estudios de Bioequivalencia comparable con el producto de referencia \nSolicitamos a la convocante, que dicho requerimiento aplique a los productos importados no obstante para productos de origen nacional sea suficiente aval la presentacion del registro sanitario del productos ofertado emitido por la DNVS, considerando que dicho requerimiento no es un requisito exigido por la agencia reguladora nacional, no obstante los registros otorgados por dicha agencia reguladora, de igual forma garantizan la calidad seguridad y eficacia con los estudios presentados para la obtencion del registro sanitario, por lo que solicitamos no limitar imnecesariamente la participacion de potenciales oferentes", "answer": "REMITIRSE A LA ADENDA N\u00b0 1 - PBC VERSI\u00d3N 2. 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