The Member States may continue to apply national transposition measures adopted under Commission Directive 2003/94/EC ( 5 ) to the manufacture of investigational medicinal products used in clinical trials governed by Directive 2001/20/EC of the European Parliament and of the Council ( 6 ) in accordance with the transitional provisions laid down in Article 98 of Regulation (EU) No 536/2014.
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 26 of Commission Delegated Regulation (EU) 2017/1569 (LawPlayer, data as of 2026-07-04)