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Regulation (EC) No 1394/2007 Article 25

Regulation (EC) No 1394/2007 Article 25

Report and review

Article 25

By 30 December 2012, the Commission shall publish a general report on the application of this Regulation, which shall include comprehensive information on the different types of advanced therapy medicinal products authorised pursuant to this Regulation. In this report, the Commission shall assess the impact of technical progress on the application of this Regulation. It shall also review the scope of this Regulation, including in particular the regulatory framework for combined advanced therapy medicinal products.

Read the full instrument → · Read this in context: CHAPTER 8 — GENERAL AND FINAL PROVISIONS →

Other provisions in CHAPTER 8 — GENERAL AND FINAL PROVISIONS

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

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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