EDQM: Update of Guideline "How to read a CEP"
In May, the first revision of the guideline "How to read a CEP (PA/PH/CEP (15) 31, 1R)" was published on the EDQM (European Directorate for the Quality of Medicines & HealthCare) website. It mainly contains updates resulting from the introduction of CEP 2.0 in 2023. The three formats of the CEP that now exist (CEP 2.0, Hybrid CEP and CEP) are clearly presented in the new version.
The guideline consists of five chapters, with chapters 4 and 5 containing further subsections. The updated guideline now contains the following structure:
1. INTRODUCTION
2. AIM AND SCOPE OF A CEP
3. GENERAL CONSIDERATIONS
4. CEP FORMATS
4.1. CEP 2.0 AND HYBRID CEP
4.1.1. NUMBERING
4.1.2. CEP LETTER OF ACCESS
4.1.3. SITES
4.2. OLD CEP
4.2.1. NUMBERING
4.2.2. DECLARATION OF ACCESS BOX
4.2.3. SITES
5. CONTENT OF CEPS
5.1. CONTENT OF CEP 2.0
5.1.1. STATEMENTS ON A CHEMICAL CEP
5.1.2. STATEMENTS ON A HERBAL CEP
5.1.3. STATEMENTS ON A TSE CEP
5.2. CONTENT OF OLD CEPS
5.2.1. STATEMENTS ON AN OLD CHEMICAL CEP
5.2.2. STATEMENTS ON AN OLD HERBAL CEP
5.2.3. STATEMENTS ON AN OLD TSE CEP
5.3. CONTENT OF A HYBRID CEP
5.3.1. STATEMENTS ON A CHEMICAL CEP
5.3.2. STATEMENTS ON A HERBAL CEP
5.3.3. STATEMENTS ON A TSE CEP
LIST OF ABBREVIATIONS
On the EDQM website you can view the updated guideline "How to read a CEP (PA/PH/CEP (15) 31, 1R)" in the "Certification Policy Documents & Guidelines" section under "General documents".
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



