Search across the website

Find training courses, blog posts, guidelines, knowledge base articles and more.

to navigate esc to close to open
GMP

The linguistic review process of product information in the centralised procedure - Human

Imported from European Medicines Agency (https://www.ema.europa.eu/en/human-regulatory/marketing-authorisation/pre-authorisation-guidance).

Organizations:
EMA

Version Timeline

Chronological release history

current

Version milestone

Publication Date

Not specified

Effective Date

Not specified