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How to submit variations in Europe MasterClass

9/16/21 8:00 AM - 9/16/21 4:00 PM
VenueOnline event

Variations are an essential part of pharmaceutical products lifecycle and a critical milestone
for the management of post-approval changes. Regulation worldwide is not yet harmonised
and this course will help you understand the specific legal framework of variations in Europe.
Through practical examples and exercices, you will learn to define the best submission strategy,
evaluate the documents to prepare and understand the challenges of implementing changes.

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