WEBINAR | Reglamento EU/2017/745 de productos sanitarios: la nueva realidad

En este webinar se revisarán cuáles son los aspectos regulatorios pre- y post-CE más impactados por la MDR, así como su estado actual de implementación.

June 15, 2021

🔹 Tras cuatro años de transición desde su publicación en el diario oficial de la Unión Europea, finalmente el 26 de mayo de este año el Reglamento EU/2017/745, también conocido como MDR (Medical Device Regulation), ha desplazado definitivamente las Directivas 93/42/EEC y 90/385/EEC como nuevo marco legal para productos sanitarios en Europa.

🔹 En este webinar, organizado por ASPHALION en colaboración con Farmaforum, se revisarán cuáles son los aspectos regulatorios pre- y post-CE más impactados por la MDR, así como su estado actual de implementación.

📆 Fecha: 29 de Junio

🕙 Hora: 10:00 a.m. (CEST)

🔹 Ponente: Dominique Monferrer, Medical Device Director

✎Inscripción:

https://www.farmaindustrial.com/conferencias/Reglamento-de-productos-sanitarios-la-nueva-realidad

✦Para cualquier información adicional, pueden contactarnos: [email protected]

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WEBINAR | Reglamento EU/2017/745 de productos sanitarios: la nueva realidad

En este webinar se revisarán cuáles son los aspectos regulatorios pre- y post-CE más impactados por la MDR, así como su estado actual de implementación.

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Related news and events

WEBINAR| Pre-clinical Testing Requirements under Regulation (EU) 2017/745 on Medical Devices: A Notified Body’s Perspective

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About

Team

Partners

CSR

AI Ethic Code

Careers

WEBINAR | Reglamento EU/2017/745 de productos sanitarios: la nueva realidad

En este webinar se revisarán cuáles son los aspectos regulatorios pre- y post-CE más impactados por la MDR, así como su estado actual de implementación.

Search

Filter by category

Related news and events

WEBINAR| Pre-clinical Testing Requirements under Regulation (EU) 2017/745 on Medical Devices: A Notified Body’s Perspective

EVENT | Health Revolution Congress

IVDR | Retos y claves del nuevo reglamento europeo

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