Regulation (EC) No 1394/2007 Article 5

Good manufacturing practice

Article 5

The Commission shall, after consulting the Agency, draw up guidelines in line with the principles of good manufacturing practice and specific to advanced therapy medicinal products.

Read the full instrument → · Read this in context: CHAPTER 2 — MARKETING AUTHORISATION REQUIREMENTS →

Other provisions in CHAPTER 2 — MARKETING AUTHORISATION REQUIREMENTS

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

What to look at next

Regulation (EC) No 1394/2007, full textChapter navigation and full text, so you can read this section in contextEuropean Union legislation EU Legal Acts by type and yearGrouped by instrument type and year of enactment, so you can find others of the same kindBrowse by type and year CHAPTER 2 — MARKETING AUTHORISATION REQUIREMENTS — read this in contextThe surrounding text of the act in order, so you can see what comes before and afterChapters and sections