English
Select your language
Official EU languages:
Access to European Union law
EUR-Lex
Access to European Union law
This document is an excerpt from the EUR-Lex website
Use quotation marks to search for an "exact phrase". Append an asterisk (*) to a search term to find variations of it (transp*, 32019R*). Use a question mark (?) instead of a single character in your search term to find variations of it (ca?e finds case, cane, care).
Need more search options? Use the
Advanced search
Document 32017R0556
Good Clinical Practice Inspections Procedures
Kommissionens gennemførelsesforordning (EU) 2017/556 af 24. marts 2017 om de nærmere bestemmelser om inspektionsprocedurerne for god klinisk praksis i henhold til Europa-Parlamentets og Rådets forordning (EU) nr. 536/2014 (EØS-relevant tekst. )
- Legal basis:
- 32014R0536 - A78P7
- EuroVoc thesaurus:
- medicinsk forskning; sundhedstilsyn; salgstilladelse; forsøg; lægemiddel; adfærdskodeks; forsøg på mennesker; lovgivning om apotekervæsen; bioetik
-
- Documents:
- Ares(2016)5693558 (Draft implementing regulation)
- Legal basis:
- 32014R0536 - A78P7
- Leading service:
- Directorate-General for Health and Food Safety
- Committee:
- Standing Committee on medicinal products for human use
- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 4
- Check the status of this initiative on the Better Regulation Portal
-
- Documents:
- C/2017/1812 final (Implementing regulation)
- Leading service:
- Directorate-General for Health and Food Safety
-
- Documents:
- 32017R0556 (Implementing regulation)
- Date of publication:
- 25/03/2017