{"id":57,"date":"2024-01-16T12:43:14","date_gmt":"2024-01-16T11:43:14","guid":{"rendered":"https:\/\/www.grupoasinfarma.churbayportillo.com\/seminario-expertos\/?page_id=57"},"modified":"2025-12-11T21:31:32","modified_gmt":"2025-12-11T20:31:32","slug":"programa-2024","status":"publish","type":"page","link":"https:\/\/www.asinfarma.com\/seminario-expertos\/procesos-esteriles-2024\/programa-2024\/","title":{"rendered":"Programa seminario expertos 2024"},"content":{"rendered":"\n

Ponencias sobre Procesos Est\u00e9riles<\/strong> previstas para los pr\u00f3ximos 7 y 8 de mayo<\/p>\n\n\n\n

Martes, 7 de mayo<\/strong><\/p>\n\n\n\n

<\/strong><\/td>INAUGURACI\u00d3N DEL SEMINARIO<\/strong><\/td><\/tr>
09:00 <\/strong><\/td>Bienvenida<\/strong>
Fernando Taz\u00f3n<\/a>, ASINFARMA<\/em><\/td><\/tr>
<\/td>CASOS REALES DE LA INDUSTRIA<\/strong><\/td><\/tr>
09:15 <\/strong><\/td>Impacto del Anexo 1: de un proceso de dosificado as\u00e9ptico convencional al uso de RABS<\/a><\/strong>
Laura Rojas<\/a>, INIBSA<\/em><\/td><\/tr>
10:00 <\/strong><\/td>Implementaci\u00f3n pr\u00e1ctica de la estrategia de control de la contaminaci\u00f3n (CCS) en la industria farmac\u00e9utica<\/a><\/strong>
\u00c0ngels Garc\u00eda<\/a>, BOEHRINGER INGELHEIM<\/em><\/td><\/tr>
10:45 <\/strong><\/td>Questions and Answers<\/strong>
Moderador: Dra. Mar Mart\u00ed<\/a>, ASINFARMA<\/em><\/td><\/tr>
11:00 <\/strong><\/td>Descanso<\/strong><\/td><\/tr>
<\/td>TECNOLOG\u00cdAS DE FUTURO EN PRODUCCI\u00d3N<\/strong><\/td><\/tr>
11:30 <\/strong><\/strong><\/td>Perfeccionando la producci\u00f3n as\u00e9ptica: uso de tecnolog\u00eda de aisladores<\/a><\/strong>
Jessica Rico<\/a>, BOEHRINGER INGELHEIM.<\/em>
Daniel Corredera<\/a>, BOEHRINGER INGELHEIM<\/em><\/td><\/tr>
12:30<\/strong><\/strong><\/strong><\/td>Future of Single Use System (SUS), towards safer, more contained & environmentally friendly processes<\/a> <\/em><\/strong>(ponencia en ingl\u00e9s)
Dario Bonanni<\/a>, MERCK<\/em><\/td><\/tr>
13:15<\/strong><\/td>Estudios de extra\u00edbles y lixiviables en productos est\u00e9riles: garantizando la calidad y seguridad farmac\u00e9utica<\/a><\/strong>
M\u00f3nica Hern\u00e1ndez<\/a>, ROVI<\/em><\/td><\/tr>
13:45 <\/strong><\/td>Questions and Answers<\/strong>
Moderador: Dra. Mar Mart\u00ed,<\/a> ASINFARMA<\/em><\/td><\/tr>
14:00<\/strong><\/td>Descanso<\/strong><\/td><\/tr>
<\/td>SISTEMA DE CALIDAD EN LA FABRICACI\u00d3N DE EST\u00c9RILES<\/strong><\/td><\/tr>
15:00<\/strong><\/strong><\/td>Dificultades en la integraci\u00f3n de la gesti\u00f3n de riesgos de calidad (QRM) en medicamentos est\u00e9riles desde el entorno de producci\u00f3n<\/a><\/strong>
Miguel \u00c1ngel G\u00f3mez<\/a>, B. BRAUN Medical<\/em><\/td><\/tr>
15:45<\/strong><\/strong><\/td>Preserving Data Integrity in Microbiology Quality Control Laboratories<\/a><\/strong><\/em> (ponencia en ingl\u00e9s)
Dr. Nicolas Leli\u00e8vre<\/a>, MECK KgAA<\/em><\/td><\/tr>
16:15<\/strong><\/td>Questions and Answers<\/strong>
Moderador: Fernando Taz\u00f3n<\/a>, ASINFARMA<\/em><\/td><\/tr>
16:30<\/strong><\/td>Fin de la jornada<\/strong><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n
<\/div>\n\n\n\n

Mi\u00e9rcoles 8 de mayo<\/strong><\/p>\n\n\n\n

<\/td> NUEVAS TECNOLOG\u00cdAS EN CONTROL DE CALIDAD MICROBIOL\u00d3GICO<\/strong><\/td><\/tr>
09:00 <\/strong><\/td>Avances en el control de la integridad de contenedores: uevo m\u00e9todos y tecnolog\u00edas de CCIT<\/a><\/strong>
Rogelio Cort\u00e9s<\/a>, ASINFARMA<\/em><\/td><\/tr>
09:45 <\/strong><\/td>Incubaci\u00f3n inteligente para el control ambiental<\/a><\/strong>
Xavier de Prado<\/a>, SENER DIAGNOSTIC<\/em><\/td><\/tr>
10:15 <\/strong><\/td>ATP-Bioluminiscencia como m\u00e9todo r\u00e1pido para el test de esterilidad y bioburden<\/a><\/strong>
Jordi Iglesias<\/a>, CHARLES RIVER<\/em><\/td><\/tr>
10:45 <\/strong><\/td>Questions and Answers<\/strong>
Moderador: Dra. Mar Mart\u00ed<\/a>, ASINFARMA<\/em><\/td><\/tr>
11:00 <\/strong><\/td>Descanso<\/strong><\/td><\/tr>
<\/td>PUNTOS CR\u00cdTICOS EN PRODUCCI\u00d3N AS\u00c9PTICA<\/strong><\/td><\/tr>
11:30 <\/strong><\/strong><\/td>Retos asociados a la implementaci\u00f3n del PUPSIT<\/a><\/strong>
Dra. Gloria Pontes<\/a>, CYTIVA SPAIN<\/em>
Raquel Llobell<\/a>, CYTIVA SPAIN<\/em><\/td><\/tr>
12:<\/strong><\/strong>00<\/strong><\/td>Optimizaci\u00f3n de las desviaciones de resultados microbianos (MDD): estrategias y puntos cr\u00edticos<\/a><\/strong>
Dra. Mar Mart\u00ed<\/a>, ASINFARMA<\/em><\/td><\/tr>
12:30<\/strong><\/td>Evoluci\u00f3n de la formaci\u00f3n del personal en la fabricaci\u00f3n de productos est\u00e9riles<\/a><\/strong>
M\u00aa Teresa Garcia<\/a>, SANDOZ<\/em><\/td><\/tr>
13:15 <\/strong><\/td>An Educational Foundation to Secure the Future of Pharma<\/a><\/strong> <\/em>(ponencia en ingl\u00e9s)
Vanessa Figueroa<\/a>, Quality Executive Partners QxP<\/em><\/td><\/tr>
13:45<\/strong><\/td>Questions and Answers<\/strong>
Moderador: Fernando Taz\u00f3n<\/a>, ASINFARMA<\/em><\/td><\/tr>
14:00<\/strong><\/td>Descanso<\/strong><\/td><\/tr>
<\/td>AUDITAR SEG\u00daN NUEVO ANEXO 1<\/strong><\/td><\/tr>
15:00<\/strong><\/strong><\/td>Primeros meses de transici\u00f3n del Anexo 1 EU GMP (2023 \u2013 2024)<\/a><\/strong>
Xavier Casterat<\/a>, NOVARTIS FARMAC\u00c9UTICA SA<\/em><\/td><\/tr>
15:45<\/strong><\/strong><\/td>Explorando experiencias: sesi\u00f3n de Q&A con expertos auditores<\/strong>
Xavier Casterat<\/a>, NOVARTIS FARMAC\u00c9UTICA SA<\/em>
Dra. M\u00aa Jes\u00fas Alonso<\/a>, ASINFARMA<\/em>
Moderador: Fernando Taz\u00f3n<\/a>, ASINFARMA<\/em><\/td><\/tr>
<\/td>CIERRE DEL SEMINARIO<\/strong><\/td><\/tr>
16:30<\/strong><\/td>Cierre y fin de la jornada<\/strong>
Fernando Taz\u00f3n<\/a>, ASINFARMA<\/em><\/td><\/tr><\/tbody><\/table><\/figure>\n","protected":false},"excerpt":{"rendered":"

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