CEP stands for
Certification of suitability of European Pharmacopoeia monographs. COS
(“Certificate of Suitability”) means the same and, even if often used, is not
the official acronym.
The role of
the CEP is to demonstrate that the purity of a given substance produced by a
given manufacturer is suitably controlled by the relevant monograph(s) of the
European Pharmacopoeia. By demonstrating that they have been
granted a CEP for their substance, suppliers of raw materials can prove this
suitability to their pharmaceutical industry clients.
CEP is granted by the Certification Secretariat of the European Directorate for the Quality of Medicines (EDQM). The CEP confirms that pharmaceutical substances or active pharmaceutical ingredients (API) are produced according to the monographs of the EP, and therefore meeting the requirements of EU directives for medicines.
Advantages of the CEP
- Full confidentiality
of the submitted data,
- Centralized
evaluation by the EDQM,
- Recognized by all
Member States of the European Pharmacopoeia Convention (36 countries) as
well as by other countries,
- Easing of the
management of applications for marketing authorization (MAA)
for medicinal products in these countries,
- Simplifies the approbation
of a medicinal product compared to the active substance master file (ASMF) or European drug master file (EDMF).
The Certificate of suitability is valid for five years from
the date when the original certificate was granted. Regardless of any revisions
treated in the meantime, the holder of a Certificate of suitability shall ask
for the renewal of the Certificate of suitability six months prior to expiry
date by providing an update of the certification dossier.
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