Posts 4 Veranstaltungen

PREFERRED

Masterclass China: Medical Device Marketing Authorisation for Advanced - New regulations on medical devices, perfection of pre-market registration an

FORUM Institut für Management GmbH (147)

- Update your regulatory knowledge - Pre-Market Registration (PMR): Minimalise your efforts and costs - Acceptance of European registration tests - Clinical pathways: From feasibility study report (FSR) to a clinical trial - Post-market Surveillance...

• Webinar
• Ohne Einstufung

• 10.09.2024 - 11.09.2024

PREFERRED

CMC Management in Regulatory Affairs - Quality data for marketing authorisation in Europe

FORUM Institut für Management GmbH (147)

- Regulatory requirements in the EU and the ICH region - Essential quality data for marketing authorisation - CMC documentation: Module 3, ASMF, CEP and Quality Overall Summary - Management of post-approval changes - Classification of quality related...

• Webinar
• Ohne Einstufung

• 12.11.2024 - 13.11.2024

PREFERRED

Medical Devices in China - Market Potential and Product Approval in China

FORUM Institut für Management GmbH (147)

- Market potential for European companies in the Chinese market - Product approval - National Medical Products Administration (NMPA): Documents, procedures, fees - tips and tricks - Clinical pathways - Post-market Surveillance & Quality Management Sy...

• Webinar
• Ohne Einstufung

• 04.06.2024 - 05.06.2024

PREFERRED

Der CMC-Manager in Regulatory Affairs - Fit in allen Qualitäts-Fragen in zwei Tagen

FORUM Institut für Management GmbH (147)

Proseminar am 18. November 2024 (optional buchbar): - CMC-Basiswissen im Einzelcoaching --- Lehrgangsinhalte am 19. - 20. November 2024: - Anforderungen an Modul 3 und CMC Writing - IMPD und Entwicklungsprojekte regulatorisch begleiten - Change Contr...

• Webinar
• Ohne Einstufung

• 19.11.2024 - 20.11.2024