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)
2005/28/EC • 32005L0028
Legal Acts - L
- Inbound citations: 14
- •
- Cited paragraphs: 2
- •
- Outbound citations: 32
Document summary
Allow our AI to generate this document's summary for you.
Please note, that it might take some time - depends on the documents length.
© European Union,
https://eur-lex.europa.eu, 1998 - 2024
Active Products: EUCJ + ECHR Data Package + Citation Analytics • Documents in DB: 398107 • Paragraphs parsed: 43931842 • Citations processed 3409255