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Commission Implementing Regulation (EU) 2025/2091 Article 4

Commission Implementing Regulation (EU) 2025/2091 Article 4

Implementation of a pharmaceutical quality system

Article 4

1.   Manufacturers shall have in place a comprehensive pharmaceutical quality system designed to ensure the quality of the veterinary medicinal products. 2.   Compliance with good manufacturing practice and the terms of the marketing authorisation shall be an essential part of the pharmaceutical quality system.

Read the full instrument → · Read this in context: CHAPTER II — PHARMACEUTICAL QUALITY SYSTEM →

Other provisions in CHAPTER II — PHARMACEUTICAL QUALITY SYSTEM

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 4 of Commission Implementing Regulation (EU) 2025/2091 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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