Quality aspects of pharmaceutical veterinary medicines for administration via drinking water - Scientific guideline
Table of contents
This document sets out the quality data requirements that are specific to veterinary medicinal products that are administered in drinking water of animals. It also provides guidance for in-use stability testing of these products.
Keywords: Veterinary medicinal product, biocides, drinking water
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Guideline on Quality Aspects of Pharmaceutical Veterinary Medicines for administration via drinking water - Draft Annex on compatibility studies between veterinary medicinal products and biocidal products (PDF/213.81 KB)
Draft: consultation open
First published: 31/03/2023
Consultation dates: 01/04/2023 to 30/06/2023
EMA/CVMP/QWP/592906/2022 -
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Concept paper on the need for amendment of Guideline on Quality Aspects of Pharmaceutical Veterinary Medicines for administration via drinking water - Annex on the concomitant use of Veterinary Medicinal Products and biocides. (PDF/132.6 KB)
Draft: consultation closed
First published: 28/01/2022
Consultation dates: 28/01/2022 to 30/04/2022
EMA/CVMP/QWP/697426/2021 -
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Guideline on quality aspects of pharmaceutical veterinary medicines for administration via drinking water (PDF/178.25 KB)
Adopted
First published: 15/04/2005
Last updated: 15/04/2005
Legal effective date: 15/01/2005
EMEA/CVMP/540/03 Rev 1