COMMISSION REGULATION (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products ANNEX ‘ANNEX VI
Changelog
0 versionsArticle-level history is being prepared
The official source publishes these consolidated versions; article-by-article changes will appear here as soon as they are processed.
No consolidated versions are recorded for this law.