Changes to 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
EU Directive 2005/28
Made by Regulation (EU) 2017/556 on the detailed arrangements for the good clinical practice inspection procedures…
| Provision | Change | Made by | In force |
|---|---|---|---|
| Directive | repeal | Regulation | — |
From legislation.gov.uk's record of changes, the official one: see it there.