Entities involved in repackaging or relabelling shall:
(a)
transfer relevant information to their customers and competent authorities in accordance with the provisions of Article 19 of Implementing Regulation (EU) 2021/1280 on good distribution practice for active substances used as starting material in veterinary medicinal products;
(b)
ensure compliance with Article 47 with regards to the certificates of analysis.
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 70 of Commission Implementing Regulation (EU) 2025/2154 (LawPlayer, data as of 2026-07-04)
