My bookmarksSign up free

Commission Regulation (EC) No 507/2006 Article 10

Commission Regulation (EC) No 507/2006 Article 10

Agency advice prior to marketing authorisation application

Article 10

A potential applicant for a marketing authorisation may request the advice of the Agency on whether a specific medicinal product being developed for a specific therapeutic indication falls within one of the categories set out in Article 2 and fulfils the requirement laid down in Article 4(1)(c).

Read the full instrument →

Other provisions in Commission Regulation (EC) No 507/2006

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 10 of Commission Regulation (EC) No 507/2006 (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.

What to look at next