Regulation · EU
Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products Text with EEA relevance
- Identifier
- CELEX 32010R1235
- Status
- in_force
- Adopted
- 15 December 2010
- Published
- 15 December 2010
- Language
- en
- Official source
- https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32010R1235
- Source provider
- eurlex
- Retrieved
- 2026-08-27T23:14:36.585Z
Identifier
- CELEX: 32010R1235 · eurlex
Direct relationships
PoliticalRepo: CELEX 32010R1235
- Identifier matchPROJECTS_FROM
Same CELEX 32010R1235 projected from PoliticalRepo EUR-Lex row 32010R1235.
LegalInstrument → PoliticalRecord · Open related record