Regulation (EC) No 1394/2007 Article 1

Subject matter

Article 1

This Regulation lays down specific rules concerning the authorisation, supervision and pharmacovigilance of advanced therapy medicinal products.

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Other provisions in CHAPTER 1 — SUBJECT MATTER AND DEFINITIONS

Article 2: Definitions

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 1 of Regulation (EC) No 1394/2007 (LawPlayer, data as of 2026-07-04)

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