CMDh/HMA: Updated Guidance Documents on Variation Notifications
Since 01 January 2025, the "Guidance Documents" regarding the updated "Variation Regulation" (Commission Delegated Regulation (EU) 2024/1701 of 11 March 2024 amending Regulation (EC) No 1234/2008 as regards the examination of variations to the terms of marketing authorizations for medicinal products for human use) in the "Variations" section of the HMA (Heads of Medicines Agencies) website are to be observed.
They include the so-called "Best Practice Guides (BPGs) for the Submission and Processing of Variations in the Mutual Recognition Procedure" in addition to a large number of other documents. These guides consist of 8 chapters, which were updated in October 2024 and are listed below:
- Chapter 1: CMDh BPG for the Allocation of the Mutual Recognition Variation Number for Type I Notifications, Type II Variations, Grouping and Worksharing
- Chapter 2: Procedure for Automatic Validation of Mutual Recognition Procedures for Variations
- Chapter 3: CMDh BPG for the Processing of Type IA Minor Variations (Notifications) in the Mutual Recognition Procedure
- Chapter 4: CMDh BPG for the Processing of Type IB Minor Variations (Notifications) in the Mutual Recognition Procedure
- Chapter 5: CMDh BPG for the Handling of Type II Variations in the Mutual Recognition Procedure
- Chapter 6: CMDh BPG for the Processing of (Super-)Grouped Applications in the Mutual Recognition Procedure
- Chapter 7: CMDh BPG on Variation Worksharing
- Chapter 8: CMDh BPG on CMDh Recommendations on Unforeseen Variations
The "Best Practice Guides (BPGs) for the Submission and Processing of Variations in the Mutual Recognition Procedure" and many other helpful documents (with and without change tracking) can be found on the HMA website.
Related GMP News
21.10.2026EMA Clarifies ESMP Reporting for Critical Medicine Shortages
20.10.2026EDQM Updates Guidance on CEP Sister File Applications
20.10.2026EDQM Revises Guidance on Electronic Submissions for CEP Applications
14.10.2026Bioassays in the United States Pharmacopoeia - Two Chapters come into Force in Spring
07.10.2026CEP 2.0: EDQM Updates Guidance on the Use of Certificates of Suitability
23.09.2026IRIS Portal: EMA expands digital Procedure Management



