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Guidance documents

This page lists the European Medicines Agency's general guidance documents relating to veterinary medicines.

If you have comments on a document that is open for consultation, use the

and send it to vet-guidelines@ema.europa.eu.

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General

Following the consultation period, the Agency finalised the reflection paper above and submitted it to the European Commission, which published it in volume 6: notice to applicants and regulatory guidelines for medicinal products for veterinary use.

Electronic submissions

As of 1 January 2017 it is mandatory for applicants to use the eSubmission Gateway / Web Client for all veterinary procedural submissions to the Agency. For more information, including links to guidance on registration with the system, see:

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