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Submitting Monographs and Revisions
Participation in European Pharmacopoeia's public standards - setting process by the pharmaceutical industry and other partners is vital to the development of authoritative, relevant European Pharmacopoeia monographs. Interested parties can participate in any of the following ways:
- Submit new draft monographs
- Review and comment on draft monographs published in PHARMEUROPA
- Propose revisions to monographs and procedures in the current official edition of the European Pharmacopoeia and submit data for proposed alternatives.
The European Pharmacopoeia encourages you to submit draft monographs. Your draft monograph will become the starting point for the official public standard. EDQM staff will involve you in a process of public review and comment in order to refine and finalise these monographs for publication in the European Pharmacopoeia.
Monographs Required:
See the priority list of items for which the EDQM requires monographs.
Monograph Submission Guidelines:
Please submit your draft monographs or email your questions on submission through the EDQM HelpDesk.
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