Directive · EU
Commission Directive 2005/28/EC of 8 April 2005 laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (Text with EEA relevance)
- Identifier
- CELEX 32005L0028
- Status
- in_force
- Adopted
- 8 April 2005
- Published
- 8 April 2005
- Language
- en
- Official source
- https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32005L0028
- Source provider
- eurlex
- Retrieved
- 2026-08-28T01:23:15.617Z
Identifier
- CELEX: 32005L0028 · eurlex
Direct relationships
PoliticalRepo: CELEX 32005L0028
- Identifier matchPROJECTS_FROM
Same CELEX 32005L0028 projected from PoliticalRepo EUR-Lex row 32005L0028.
LegalInstrument → PoliticalRecord · Open related record