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GMP

IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants

Imported from European Medicines Agency (https://www.ema.europa.eu/en/regulatory-and-procedural-guideline.xml).

Organizations:
EMA

Version Timeline

Chronological release history

2026-09-01

Version milestone

Publication Date

Sep 1, 2026

Effective Date

Not specified