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Sin embargo, considerando que en el mercado existen indistintamente productos de origen nacional e importados para los solicitados en el presente proceso, recomendamos a la Convocante establecer para los productos importados el requerimiento de la presentaci\u00f3n del Certificado de Buenas Pr\u00e1cticas emitido por un pa\u00eds de alta y/o adecuada vigilancia conforme a la Ley 3283/07 para especialidades farmac\u00e9uticas, consider\u00e1ndose este un requisito ineludible para la obtenci\u00f3n del registro sanitario y para garantizar la calidad, seguridad y eficacia de los productos importados a ser comercializados en el pa\u00eds. Teniendo en cuenta que con esto la Convocante garantiza que el fabricante del producto ofertado cumple con los requisitos t\u00e9cnicos y legales para la elaboraci\u00f3n y posterior comercializaci\u00f3n del producto como lo hacen las empresas que cuentan con fabricaci\u00f3n nacional. De esta manera, la Convocante garantiza la participaci\u00f3n en igualdad de condiciones para todos los oferentes, oferten estos productos de origen nacional o importado.", "author": {"name": "QUIMFA S.A.", "id": "PY-RUC-80074991-0"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:28:41-04:00"}, {"id": "3", "date": "2022-07-21T14:41:17-04:00", "title": "6. Declaraci\u00f3n de miembros. ", "description": "Consulto. Al no ser requisito la DD:JJ: de la ley 6355,  este formulario, seguir\u00e1 vigente? ", "author": {"name": "Bioethic Pharma S.A.", "id": "PY-RUC-80058902-5"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC y a la Circular DNCP N\u00b0 10/2022.-", "dateAnswered": "2022-08-08T15:58:17-04:00"}, {"id": "15", "date": "2022-07-24T18:45:11-04:00", "title": "Capacidad Tecnica", "description": "En los requisitos de capacidad t\u00e9cnica se observa que la Convocante ha realizado las previsiones necesarias para que los oferentes que ofertan productos de origen nacional presenten todas las documentaciones que avalan el cumplimiento de la normativa nacional, garantizando de esta manera la calidad, eficacia y seguridad de los productos fabricados en el territorio nacional. Sin embargo, considerando que en el mercado existen indistintamente productos de origen nacional e importados para los solicitados en el presente proceso, recomendamos a la Convocante establecer para los productos importados el requerimiento de la presentaci\u00f3n del certificado de libre venta o registro sanitario del producto ofertado emitido por un pa\u00eds de alta y/o adecuada vigilancia conforme a la Ley 3283/07 para especialidades farmac\u00e9uticas, consider\u00e1ndose este un requisito ineludible para la obtenci\u00f3n del registro sanitario de productos importados. Teniendo en cuenta que con esto la Convocante garantiza que el fabricante del producto ofertado cumple con los requisitos t\u00e9cnicos y legales para la elaboraci\u00f3n y posterior comercializaci\u00f3n del producto como lo hacen las empresas que cuentan con fabricaci\u00f3n nacional. De esta manera, la Convocante garantiza la participaci\u00f3n en igualdad de condiciones para todos los oferentes, oferten estos productos de origen nacional o importado.", "author": {"name": "QUIMFA S.A.", "id": "PY-RUC-80074991-0"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:28:03-04:00"}, {"id": "1", "date": "2022-07-21T13:55:27-04:00", "title": "Ley 6355 ", "description": "5-Constancia de presentaci\u00f3n de la Declaraci\u00f3n Jurada de bienes y rentas, activos y pasivos ante la\nContralor\u00eda General de la Rep\u00fablica, para los sujetos obligados seg\u00fan los incisos a) y b) del numeral 2 del\nart. 1 de la Ley N\u00b0 6355/19. (**) Seg\u00fan ley N\u00b0 6919/22, este requisito ya no es necesario. solicito a la convocante dejar sin efecto este requisito. ", "author": {"name": "Bioethic Pharma S.A.", "id": "PY-RUC-80058902-5"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T15:46:20-04:00"}, {"id": "14", "date": "2022-07-23T20:11:27-04:00", "title": "Requisitos documentales para evaluaci\u00f3n de las condiciones de participaci\u00f3n", "description": "Teniendo en cuenta el punto N\u00ba 5 del apartado mencionado donde se solicita Constancia de presentaci\u00f3n de la Declaraci\u00f3n Jurada de bienes y rentas, activos y pasivos ante la Contralor\u00eda General de la Rep\u00fablica, para los sujetos obligados en el marco de la Ley N\u00b0 6355/19. Pedimos a la convocante que dicho requisito sea excluido en raz\u00f3n a la publicaci\u00f3n de la Circular DNCP N\u00b0 10/2022 de fecha 18 de Julio, donde se deroga dicha ley, en la misma se manifiesta que los sujetos individualizados en los incisos a) y b) del numeral 2 del art. 1 de la Ley N\u00ba 6355/19 ya no se encuentran obligados a la presentaci\u00f3n de la constancia que acredita la presentaci\u00f3n de la declaraci\u00f3n jurada de bienes y rentas, activos y pasivos en los procedimientos de contrataciones p\u00fablicas y que las Convocantes no podr\u00e1n exigir la misma.", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:26:38-04:00"}, {"id": "9", "date": "2022-07-23T19:00:34-04:00", "title": "Requisito documental para evaluar la capacidad t\u00e9cnica", "description": "Solicitamos a la convocante incluir como requisito documental la presentaci\u00f3n de la Copia Vigente del Certificado de Registro sanitario del producto ofertado; o copia Vigente del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n, Legalizada y/o apostillada o declaraci\u00f3n jurada del titular del registro sanitario emitido en Paraguay, donde se identifique el link web oficial del CERTIFICADO DE BUENAS PRACTICAS DE FABRICACION VIGENTE O REGISTRO SANITARIO VIGENTE, otorgado por alguna de las Agencias reguladoras previstas en el art\u00edculo 11 de la Ley N\u00b0 3283/07 o Agencias reguladoras de la EMA (European Medicines Agency) o FDA o Agencias Reguladoras de Referencia (Nivel 4) reconocidas por la OPS, esto a fin de brindar las garant\u00edas necesarias a los pacientes a quienes les ser\u00e1n administrados los medicamentos solicitados.", "author": {"name": "BIOTENG S.A.", "id": "PY-RUC-80035226-2"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:22:32-04:00"}, {"id": "5", "date": "2022-07-22T15:20:58-04:00", "title": "CONSULTA 2 \u0096 VENCIMIENTO ", "description": "El Pliego de Bases y Condiciones en su apartado: SUMINISTROS REQUERIDOS - ESPECIFICACIONES T\u00c9CNICAS, apartado, detalle de los productos con las respectivas especificaciones t\u00e9cnicas VENCIMIENTO se solicita cuanto sigue: \u0085 Vencimiento: El vencimiento m\u00ednimo medicamentos no deber\u00e1 ser inferior a 18 meses (diez y ocho) meses al momento de la entrega en los parques sanitarios, 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 Instituto Nacional de Ablaci\u00f3n y Trasplante. Para productos con vencimiento menor a 18 (Diez y ocho) meses adem\u00e1s de la autorizaci\u00f3n de la Direcci\u00f3n Log\u00edstica de la DGGIES y por el Instituto Nacional de Ablaci\u00f3n y Trasplante (INAT), se deber\u00e1 presentar P\u00f3liza de Seguro por el 100% del monto del producto con identificaci\u00f3n del n\u00famero de Lote; que ser\u00e1n entregados en la Oficina de Contrato y Garant\u00edas de la DGGIES y el duplicado en el Parque Sanitario que corresponda. La validez de dicha p\u00f3liza deber\u00e1 ser por 3 meses posteriores a la fecha del vencimiento del producto a entregar. Adem\u00e1s, deber\u00e1n presentar Declaraci\u00f3n Jurada por la cual el oferente se compromete en caso de ser adjudicados a canjear el producto 3 a 6 meses antes de su vencimiento, previo informe de los responsables de la Direcci\u00f3n Log\u00edstica de la DGGIES y por el Instituto Nacional de Ablaci\u00f3n y Trasplante (sic).  Considerando que: Los \u00edtems objeto de este llamado se tratan de productos biol\u00f3gicos que se obtienen mediante el empleo de organismos o c\u00e9lulas vivas, cuyo vencimiento te\u00f3rico no supera los 24 meses debido a esta condici\u00f3n, y que a su vez, pasa por rigurosos procesos de aseguramiento de calidad para asegurar la eficacia y la estabilidad del producto que pueden extenderse hasta 4 meses, sumado al tiempo de tr\u00e1nsito y desaduanaje que en promedio se extiende tambi\u00e9n por otros 4 meses para poder entregar los productos a la Convocante en tiempo y forma.  Para poder cumplir con el plan de entregas establecido por el pliego de bases y condiciones requiere contar con un stock de seguridad para dar respuesta inmediata a las necesidades de la Convocante.  El requerimiento de una p\u00f3liza de seguro para medicamentos con vencimiento mayor a 18 meses podr\u00eda incidir de forma negativa en la estructura de costos del proceso. Solicitamos que: La Convocante analice la posibilidad de modificar su segundo p\u00e1rrafo, solicitando Carta Compromiso de Canje y P\u00f3liza de Seguro por el 100% del monto del producto a ser entregado, para productos con vencimiento inferior a 12 meses.", "author": {"name": "EXXEL TECHNOLOGIES S.A.E.", "id": "PY-RUC-80024779-5"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:08:48-04:00"}, {"id": "17", "date": "2022-07-24T18:57:51-04:00", "title": "Vencimiento de los productos", "description": "En el apartado de referencia, la Convocante establece que el vencimiento m\u00ednimo medicamentos no deber\u00e1 ser inferior a 18 meses (diez y ocho) meses al momento de la entrega. Adem\u00e1s incluye que para productos con vencimiento menor a 18 (Diez y ocho) meses adem\u00e1s de la autorizaci\u00f3n de la Direcci\u00f3n Log\u00edstica de la DGGIES y por el Instituto Nacional de Ablaci\u00f3n y Trasplante (INAT), se debe presentar una P\u00f3liza de Seguro por el 100% del monto del producto. Al respecto, y considerando que la estabilidad de los productos a cotizar en su gran mayoria corresponde a un plazo de 24 meses desde su fabricaci\u00f3n, por lo que a fin de no tener un corte de stock es necesario mantener un inventario constante de los productos, tornandose de muy dificil cumplimiento contar con el vencimiento requerido y teniendo en cuenta el costo administrativo que implica el mantenimiento de polizas. Solicitamos a la Convocante tenga a bien rever la posibilidad de establecer el requerimiento de la presentaci\u00f3n de una poliza recien para productos con un vencimiento menor a 12 meses. ", "author": {"name": "QUIMFA S.A.", "id": "PY-RUC-80074991-0"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:29:32-04:00"}, {"id": "8", "date": "2022-07-23T18:57:28-04:00", "title": "Requisito documental para evaluar la capacidad t\u00e9cnica", "description": "Para el \u00edtem N\u00ba 3 Micofenolato mofetil \u0096 Comprimido solicitamos a la convocante que incluya como requisito de evaluaci\u00f3n la presentaci\u00f3n de estudio de Bioequivalencia comparable con el producto de referencia (Se entender\u00e1 por producto de referencia a aquel que se encuentre autorizado por una agencia regulatoria de alta vigilancia sobre la base de datos completos de calidad, seguridad y eficacia) esto en atenci\u00f3n a que el producto solicitado es utilizado para pacientes trasplantados.", "author": {"name": "BIOTENG S.A.", "id": "PY-RUC-80035226-2"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:21:26-04:00"}, {"id": "2", "date": "2022-07-21T13:57:09-04:00", "title": "6. Declaraci\u00f3n de miembros. ", "description": "Consulto. Al no ser requisito la DD:JJ: de la ley 6355,  este formulario, seguir\u00e1 vigente? ", "author": {"name": "Bioethic Pharma S.A.", "id": "PY-RUC-80058902-5"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC y a la Circular DNCP N\u00b0 10/2022.-", "dateAnswered": "2022-08-08T15:58:03-04:00"}, {"id": "13", "date": "2022-07-23T20:09:45-04:00", "title": "Requisitos de capacidad t\u00e9cnica", "description": "Solicitamos a la Convocante incluir como requisito para evaluar la capacidad t\u00e9cnica la presentaci\u00f3n de estudios de Bioequivalencia comparable con el producto de referencia a modo de asegurar la calidad, seguridad y eficacia de los productos ofertados.", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:25:44-04:00"}, {"id": "12", "date": "2022-07-23T20:08:26-04:00", "title": "Requisitos de capacidad t\u00e9cnica", "description": "Se solicita a la convocante la inclusi\u00f3n del siguiente requisito: Presentar Copia Legalizada y/o apostillada o declaraci\u00f3n jurada del fabricante (debidamente legalizada y/o apostillada) con el link web oficial del Certificado de Buenas Pr\u00e1cticas de Fabricaci\u00f3n vigente o Registro Sanitario, otorgado por alguna de las Agencias regulatorias previstas en el art\u00edculo 11 de la Ley N\u00b0 3283/07 o Agencias reguladoras de la EMA (European Medicines Agency) o FDA (Food and Drug Administration) o Agencias Reguladoras de Referencia (Nivel 4) reconocidas por la OPS.", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:24:31-04:00"}, {"id": "10", "date": "2022-07-23T19:03:47-04:00", "title": "Requisito documental para evaluar la capacidad t\u00e9cnica", "description": "Para el \u00edtem N\u00ba 6 Tacrolimus capsula solicitamos a la convocante que incluya como requisito de evaluaci\u00f3n la presentaci\u00f3n de estudio de Bioequivalencia comparable con el producto de referencia (Se entender\u00e1 por producto de referencia a aquel que se encuentre autorizado por una agencia regulatoria de alta vigilancia sobre la base de datos completos de calidad, seguridad y eficacia) esto en atenci\u00f3n a que el producto solicitado es utilizado para pacientes trasplantados.", "author": {"name": "BIOTENG S.A.", "id": "PY-RUC-80035226-2"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:23:16-04:00"}, {"id": "6", "date": "2022-07-22T15:21:50-04:00", "title": "CONSULTA 3 \u0096 PLAZO DE ENTREGA: ", "description": "El Pliego de Bases y Condiciones en el punto plan de entregas de los bienes, apartado Cronograma de  Entrega,  solicita cuanto sigue; \u0085Cronograma de Entrega.// Las \u00f3rdenes de compra ser\u00e1n emitidas por la Direcci\u00f3n General de Gesti\u00f3n de Insumos Estrat\u00e9gico en Salud, seg\u00fan necesidad y stock del Instituto Nacional de Ablaci\u00f3n y Trasplante. Los plazos ser\u00e1n computados en d\u00edas corridos. El proveedor deber\u00e1 tener la capacidad para realizar entregas fraccionadas, la recepci\u00f3n en cuanto a cantidades y plazos se realizar\u00e1 de la siguiente manera: Cantidades: 1) Hasta 30% de la cantidad m\u00ednima adjudicada: La primera Orden de Compra ser\u00e1 emitida dentro de los 15 (quince) d\u00edas corridos posteriores a la firma del contrato, donde el proveedor tendr\u00e1 hasta los 10 (diez) d\u00edas corridos para la entrega, contados a partir de la recepci\u00f3n de la Orden de Compra, emitida por la Direcci\u00f3n General de Gesti\u00f3n de Insumos Estrat\u00e9gicos en Salud, seg\u00fan necesidad y stock del Instituto Nacional de Ablaci\u00f3n y Trasplante. 2) Hasta el 30%de la cantidad m\u00ednima adjudicada: El proveedor tendr\u00e1 hasta los 15 (Quince) d\u00edas corridos para la entrega, contados a partir de la recepci\u00f3n de la Orden de Compra, emitida por la Direcci\u00f3n General de Gesti\u00f3n de Insumos Estrat\u00e9gicos en Salud, seg\u00fan necesidad y stock del Instituto Nacional de Ablaci\u00f3n y Trasplante. 3 ) Saldo de la cantidad m\u00ednima La emisi\u00f3n de la Orden de Compra se realizar\u00e1 dentro de los 6 (seis) meses posteriores a la firma del Contrato. El proveedor tendr\u00e1 hasta los 15 (quince) d\u00edas corridos para la entrega contados a partir de la recepci\u00f3n de la Orden de Compra emitida por la Direcci\u00f3n General de Gesti\u00f3n de Insumos Estrat\u00e9gicos en Salud, seg\u00fan necesidad y stock del Instituto Nacional de Ablaci\u00f3n y Trasplante. Cantidades M\u00e1ximas. La emisi\u00f3n de la Orden de Compra se realizar\u00e1 hasta el 31/12/2024. Ser\u00e1n fraccionadas seg\u00fan necesidad de los servicios, tendr\u00e1 hasta 20 d\u00edas corridos para la entrega de los productos que le fueran adjudicados en el\npresente llamado (sic). Considerando que: estos productos deben ser importados y que por la naturaleza de los mismos  su vencimiento te\u00f3rico no superan los 24  meses y que a su vez, pasan por rigurosos procesos de aseguramiento de calidad para asegurar la eficacia y la estabilidad del producto que pueden extenderse hasta  4  meses, sumado al tiempo de tr\u00e1nsito y desaduanaje por la coyuntura actual por la que se atraviesa a nivel global, por la disminuci\u00f3n de los itinerarios a\u00e9reos y las escasa disponibilidad de espacio en las aeronaves, los cuales  generan dilaciones significativas en las importaciones. En este sentido, solicitamos a la Convocante analice la posibilidad de establecer el siguiente plan de entregas:  CANTIDAD MINIMA: - Primera Entrega Hasta el 30 % de la Cantidad M\u00ednima Adjudicada. Hasta los 20 (veinte) d\u00edas corridos contados desde la recepci\u00f3n de la Orden de compra por parte del proveedor. Con entregas que podr\u00e1n ser fraccionadas siempre dentro del mencionado plazo. \u0096  Segunda Entrega: Hasta el 30 % de la Cantidad M\u00ednima adjudicada: Hasta los 25 (veinte y cinco) d\u00edas corridos, contados desde la recepci\u00f3n de la Orden de compra por parte del proveedor. Con entregas que podr\u00e1n ser fraccionadas siempre dentro del mencionado plazo. Cantidades m\u00e1ximas Las cantidades m\u00e1ximas podr\u00e1n ser fraccionadas seg\u00fan necesidad y stock de los servicios tendr\u00e1 hasta 30 (treinta) d\u00edas corridos para la entrega a partir de la recepci\u00f3n de la Orden de compras emitida por la DGGIES seg\u00fan necesidad y stock de los hospitales de referencia en el cual ser\u00e1n tratados los pacientes.\n", "author": {"name": "EXXEL TECHNOLOGIES S.A.E.", "id": "PY-RUC-80024779-5"}, "answer": "La convocante se mantiene en los t\u00e9rminos inicialmente establecido en el PBC, aclarando a  que se debe a la importancia de contar con los medicamentos en la brevedad posible, bien sabido que la falta de acceso y consumo de estos medicamentos para los pacientes trasplantados puede llevar al rechazo y perdida del \u00d3rgano trasplantado poniendo en riesgo incluso la vida del mismo.", "dateAnswered": "2022-08-08T17:17:59-04:00"}, {"id": "7", "date": "2022-07-22T15:22:45-04:00", "title": "CONSULTA 4 \u0096 REQUISITOS DE CALIDAD: ", "description": "El Pliego de Bases y Condiciones en el apartado Requisito documental para evaluar la capacidad t\u00e9cnica, solicitamos a la convocante analice la posibilidad de incluir entre los requisitos los siguientes documentos de referencia, a) En caso de oferentes de productos importados, se deber\u00e1 presentar copias debidamente legalizada o apostilladas de los Certificados de Registro Sanitario y/o autorizaci\u00f3n de comercializaci\u00f3n (CLV), vigentes, otorgados por las Agencias Reguladoras prevista en el Art. 11 de la Ley 3283/07 o Agencias Reguladoras de referencia (nivel 4) reconocidas por la OPS  b), Estudio de Bioequivalencia comparable con el producto innovador de referencia, esto debido a que el mismo es fruto del proceso de investigaci\u00f3n y desarrollo, y por ello posee la  experiencia de comercializaci\u00f3n m\u00e1s larga, demostrando  el continuo uso cl\u00ednico", "author": {"name": "EXXEL TECHNOLOGIES S.A.E.", "id": "PY-RUC-80024779-5"}, "answer": "Ajustarse a la \u00faltima versi\u00f3n del PBC.-", "dateAnswered": "2022-08-08T17:20:23-04:00"}, {"id": "4", "date": "2022-07-22T15:20:30-04:00", "title": "CONSULTA 1:  ESPECIFICACIONES TECNICAS - ITEM 3:", "description": "El Pliego de Bases y Condiciones en su apartado: SUMINISTROS REQUERIDOS - ESPECIFICACIONES T\u00c9CNICAS, apartado, detalle de los productos con las respectivas especificaciones t\u00e9cnicas en el \u00cdtem 3 (MICOFENOLATO DE MOFETILO- COMPRIMIDO), t\u00edtulo DESCRIPCI\u00d3N, prev\u00e9 cuanto sigue: \u0085 Comprimido (Sic). Ahora bien, considerando que la presentaci\u00f3n  tabletas recubiertas, mejora la estabilidad del producto ante la humedad, oxigeno, di\u00f3xido de carbono y  mejora la biodisponibilidad del f\u00e1rmaco,   as\u00ed como facilita la digesti\u00f3n del mismo por parte del paciente protegiendo la membrana g\u00e1strica,  se solicita a la Convocante analice la posibilidad adem\u00e1s  de incluir la forma farmac\u00e9utica en tabletas recubiertas, esto a fin de garantizar adem\u00e1s una mayor participaci\u00f3n de potenciales oferentes, respetando as\u00ed los principios de igualdad y libre competencia previsto en la Ley 2051/03. ", "author": {"name": "EXXEL TECHNOLOGIES S.A.E.", "id": "PY-RUC-80024779-5"}, "answer": "La convocante aclara que la forma farmac\u00e9utica comprimido recubierto y tableta recubierta son sin\u00f3nimos.", "dateAnswered": "2022-08-08T17:08:14-04:00"}], "lots": [{"id": "6vIBITELeXI=", "title": "7 - Basiliximab Inyectable", "status": "complete", "statusDetails": "Cerrado Con Lances", "value": {"amount": 749940450, "currency": "PYG"}, "openContractType": " Por cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "7", "id": "1"}]}, {"id": "Gcw7y3tiEug=", "title": "4 - Inmunoglobulina de Conejo Antitimocito Humano Inyectable", "status": "complete", "statusDetails": "Cerrado Con Lances", "value": {"amount": 2803085600, "currency": "PYG"}, "openContractType": " Por cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "4", "id": "1"}]}, {"id": "7EsY/VuWjlo=", "title": "2 - Ciclosporina - C\u00e1psula", "status": "complete", "statusDetails": "Cerrado Con Lances", "value": {"amount": 178230000, "currency": "PYG"}, "openContractType": " Por cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "2", "id": "1"}]}, {"id": "0E7c2NH+k1Q=", "title": "8 - 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Tacrolimus capsula", "status": "complete", "statusDetails": "Cerrado Con Lances", "value": {"amount": 28987000000, "currency": "PYG"}, "openContractType": " Por cantidad", "simultaneousSupply": true, "attributes": [{"name": "Orden", "value": "6", "id": "1"}]}], "items": [{"id": "y4dAyJ/DkJIpTwTN6uK3nQ==", "description": "Ciclosporina - Soluci\u00f3n Bebible", "classification": {"scheme": "catalogoNivel5DNCP", "id": "51201502-002", "description": "Ciclosporina - Soluci\u00f3n Bebible", "uri": "https://www.contrataciones.gov.py/datos/api/v3/doc/itemClassification/n5/51201502-002"}, "additionalClassifications": [{"scheme": "UNSPSC", "id": "51201502", "description": "Ciclosporina", "uri": "https://www.contrataciones.gov.py/datos/api/v3/doc/itemClassification/n4/51201502"}], "quantity": 40, "minQuantity": 20, "unit": {"name": "Unidad", "id": "UNI", "value": {"amount": 1200000, "currency": "PYG"}}, "relatedLot": "qvJ/09Balp8=", "attributes": [{"name": "Presentacion", "value": "FRASCO", "id": "1"}, {"name": "Orden", "value": "1", "id": "2"}]}, {"id": "htg+DvsvPX/PA8308m88rQ==", "description": "Ciclosporina - 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