art_15__para_3__point_f__text_1 — Regulation (EU) 2022/123 of the European Parliament and of the Council of 25… · Lexiara

art_15__para_3__point_f__text_1

Regulation (EU) 2022/123 of the European Parliament and of the Council of 25 January 2022 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices (Text with EEA relevance) · European Union

other clinical trial experts who represent national competent authorities for medicinal products.

← (f) · All articles · art_15__para_3__text_2 →

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