44. — Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16… · Lexiara

44.

Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC Text with EEA relevance · European Union

The IMPD shall contain a statement of the good laboratory practice status or equivalent standards, as referred to in Article 25(3).

← anx_I__cpt_7__cpt_1__cpt_3__point_43__text_1 · All articles · anx_I__cpt_7__cpt_1__cpt_3__point_44__text_1 →

Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.