European Shortages Monitoring Platform (ESMP): Stakeholder engagement plan
Submitted by Anonymous (not verified) on 10 December 2024 - 14:18
European Shortages Monitoring Platform (ESMP): Stakeholder engagement plan
Methodology European Specialised Expert Community (ESEC): Members
Submitted by Anonymous (not verified) on 10 December 2024 - 14:15
Methodology European Specialised Expert Community (ESEC): Members
Three-year rolling work plan for the Quality Innovation Group (QIG) 2025-2027
Submitted by Anonymous (not verified) on 10 December 2024 - 14:09
Three-year rolling work plan for the Quality Innovation Group (QIG) 2025-2027
Clinical trial information system (CTIS) public portal full trial information
Submitted by Anonymous (not verified) on 10 December 2024 - 13:57
Clinical trial information system (CTIS) public portal full trial information
Clinical trial information system (CTIS) public portal trial results
Submitted by Anonymous (not verified) on 10 December 2024 - 13:56
Clinical trial information system (CTIS) public portal trial results
IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants
Submitted by Anonymous (not verified) on 10 December 2024 - 13:46
IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants
Regulatory Procedure Management (RPM) for the Product Lifecycle Management (PLM) - Frequently asked questions
Submitted by Anonymous (not verified) on 10 December 2024 - 13:30
Regulatory Procedure Management (RPM) for the Product Lifecycle Management (PLM) - Frequently asked questions
Frequently asked questions on the European Shortages Monitoring Platform (ESMP)
Submitted by Anonymous (not verified) on 10 December 2024 - 13:25
Frequently asked questions on the European Shortages Monitoring Platform (ESMP)
Guidance notes on the use of Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) terminology for reporting suspected adverse events in animals and humans - Rev.16
Submitted by Anonymous (not verified) on 10 December 2024 - 13:15
Guidance notes on the use of Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) terminology for reporting suspected adverse events in animals and humans - Rev.16
Agenda - PDCO agenda of the 10-13 December 2024 meeting
Submitted by Anonymous (not verified) on 10 December 2024 - 13:03
Agenda - PDCO agenda of the 10-13 December 2024 meeting