
Inês Vaz
18 March 2026
Understanding EU Regulatory Affairs
8-hour
Regulatory affairs during product development, Review regulatory affairs during non-clinical, Examine regulatory affairs during clinical studies, MAA – Regulatory submission procedures, MAA – The registration dossier, MAA – Labelling and packaging, Post approval activities and Reviewing pharmacovigilance
Adriaan Fruijtier
ISV
Issued to
Inês Vaz
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Credential Verification
Issue date: March 18, 2026
ID: 661012df-70ca-46d0-9c8f-e40caa7ac8ae
Type
Course
Level
Professional
Price
Paid
Earning Criteria
Participation
Attended the course held by Educo Life Sciences.
Watching
Or watched the recorded materials for the course held by Educo.