# Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use, Article 20

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

The Commission shall adapt this Directive to take account of scientific and technical progress.
Those measures, designed to amend non-essential elements of this Directive, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 21(3).

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Source: https://www.legislation.gov.uk/eudr/2001/20/article/20 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-20/article-20
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.