# 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), Signature

Extent: E+W+S+N.I.

Done at Brussels, 8 April 2005.
For the Commission
Günter Verheugen
Vice-President

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Source: https://www.legislation.gov.uk/eudr/2005/28/signature (the official version)
Page: https://openlegislation.uk/eu-directive-2005-28/signature
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.