As an Observer Member of VICH (the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products), we are inviting comments through a public consultation on a draft guideline relating to the technical requirements for studies demonstrating pharmaceutical development for veterinary medicinal products (VICH Quality Guideline 61).
The proposed draft document is published on the VICH website.
The consultation is open until 15 August 2024.
Comments should be relevant to this specific guideline, and can either be general on the approach outlined or comments on the actual text of the guideline.
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