List of medicinal products under additional monitoring
Submitted by Anonymous (not verified) on 24 February 2025 - 16:25
List of medicinal products under additional monitoring
List of medicinal products under additional monitoring
Submitted by Anonymous (not verified) on 24 February 2025 - 16:24
List of medicinal products under additional monitoring
New Approach Methodologies EU-IN Horizon Scanning Report
Submitted by Anonymous (not verified) on 24 February 2025 - 14:21
New Approach Methodologies EU-IN Horizon Scanning Report
Annex to 24-27 February 2025 CHMP Agenda
Submitted by Anonymous (not verified) on 24 February 2025 - 13:50
Annex to 24-27 February 2025 CHMP Agenda
Agenda of the CHMP meeting 24-27 February 2025
Submitted by Anonymous (not verified) on 24 February 2025 - 13:47
Agenda of the CHMP meeting 24-27 February 2025
Good manufacturing practice
Submitted by Anonymous (not verified) on 24 February 2025 - 13:01
Good manufacturing practice
Good distribution practice
Submitted by Anonymous (not verified) on 24 February 2025 - 13:01
Good distribution practice
Review of transparency rules for the EU Clinical Trials Information System (CTIS)
Submitted by Anonymous (not verified) on 24 February 2025 - 12:30
Review of transparency rules for the EU Clinical Trials Information System (CTIS)
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes
Submitted by Anonymous (not verified) on 24 February 2025 - 11:00
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
Submitted by Anonymous (not verified) on 24 February 2025 - 11:00
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure