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Participate in the Work of the European Pharmacopoeia
Participation in the European Pharmacopoeia's public standards setting process by the pharmaceutical industry and other stakeholders is vital for the development of authoritative and relevant European Pharmacopoeia monographs. Interested parties can participate in the following ways:
Submit Draft Monographs
The European Pharmacopoeia encourages you to submit draft monographs. Your draft may be the starting point for an official public standard.
Propose Revisions to Existing General Chapters and Monographs
You can propose revisions to the general chapters and monographs in the current official edition of the European Pharmacopoeia. Submission of data for proposed alternatives is highly welcomed to allow for proper evaluation of your proposal.
Comment in Pharmeuropa
You can comment on general texts and draft monographs published in Pharmeuropa.
In all of the above cases, EDQM staff will involve you in a process of public review of the draft text in order to refine the proposals and to publish an official text in the European Pharmacopoeia.
Products & Services
Pharmeuropa
For more information:
- Pharmeuropa and Pharmeuropa Bio & Scientific Notes
To order this publication:
- EDQM Online Store
Technical Guide for the Elaboration of Monographs of the European Pharmacopoeia (2008)
To order this publication:
- EDQM Online Store
Important Information
To download all the technical guides:
- Technical Guides
Additional Information & Documentation
For information on the procedure about submitting draft monographs or revisions, please go to the Frequently Asked Questions (FAQs) & EDQM HelpDesk.
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