Seminare zu Pharma / Medical devices
Pharma / Medical devices
High-quality courses and training for pharma
and healthcare professionals

Results FOR "Pharma / Medical devices"

SORT RESULTS

Global Regulatory Affairs Manager

This online training addresses the needs of regulatory affairs managers dealing with marketing authorisations outside the EU or planning to do so in the future.

  • Modular e-Learning and webcast / Access possible at any time

Development Expert Biologics

  • Modular e-Learning and webcast / Access possible at any time

PharmaFORUM Webcast Biologics "Pharmaceutical Development of Biologics Drug Products: the interface of formulation, primary packaging and application"

Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.

  • Online /

PharmaFORUM Webcast International "Clinical trials in China"

Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!

  • Online /

Marketing Authorisation in Latin America

A course to discuss real cases/challenges for marketing authorisation in Mexico, Argentina, Colombia, Peru, Chile and Brazil with local experts from Brazil and Spain.

  • Frankfurt-Raunheim / 23. - 24.09.2019

CMC Management in Regulatory Affairs

This course will give you an in-depth knowledge on the CMC requirements for the marketing authorisation.

  • Amsterdam / 25. - 26.09.2019

PharmaFORUM Webcast Biologics "CMC lifecycle management: ICH Q12 and others"

Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.

  • Online /

Vendor Oversight in a regulatory environment

Effective oversight of outsourced activities in the healthcare sector - Prepare yourself for the balancing act between compliance and outsourcing, and learn how to implement your own effective regulatory vendor oversight programme.

  • Berlin / 08. - 09.10.2019

CMC Documents: Scientific Writing for Regulatory Submission

How to write the Module 3 for Regulatory Submission - Here you will get in-depth information.

  • Köln / 11.10.2019

Marketing Authorisation in ASIA

Basic and advanced know-how on the current regulatory framework of the various countries will be addressed in this course.

  • Mannheim / 22. - 24.10.2019
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