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European Union
Commission Implementing Regulation (EU) 2017/556
Chapter IV
Article 15

Commission Implementing Regulation (EU) 2017/556

In forceThis text since 1 Jan 1001law://eu/reg/2017/556/art_15@2026-11-12

Version in force onWhereEuropean Union

Article 15Repeal#

Directive 2005/28/EC is repealed from the date referred to in the second paragraph of Article 17.

Source: EUR-Lex, © European Union, 1998-2026. Reuse authorised under Decision 2011/833/EU.

Key facts

Type: Implementing regulation · Commission Implementing Regulation (EU) 2017/556 · EEA relevant
In force: 1 Jan 1001
Adopted: 24 Mar 2017
Applies from: 14 Apr 2017
Made by: Directorate-General for Health and Food Safety, European Commission
Official: EUR-Lex 32017R0556 · ELI

Topics

bio-ethics code of conduct experiment on humans health control market approval medical research medicinal product pharmaceutical legislation testing Internal market - Principles Medicinal products Public health

History · 1 version

1 Jan 1001Reading

Connections

Cites 2: 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); this act