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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 23 CELEX: 02001L0020-20220101 Entry into force
This Directive shall enter into force on the day of its publication in the Official Journal of the European Communities. |