Entry into force
Article 23
This Directive shall enter into force on the day of its publication in the Official Journal of the European Communities.
Directive 2001/20/EC of the European Parliament and of the… Article 23
Directive 2001/20/EC of the European Parliament and of the… Article 23
Other provisions in Directive 2001/20/EC of the European Parliament and of the…
- Article 14: Labelling
- Article 15: Verification of compliance of investigational medicinal products with good clinical and manufacturing practice
- Article 16: Notification of adverse events
- Article 17: Notification of serious adverse reactions
- Article 18: Guidance concerning reports
- Article 19: General provisions
- Article 20: Adaptation to scientific and technical progress
- Article 21: Committee procedure
- Article 22: Application
- Article 24: Addressees
CitationArticle 23 of Directive 2001/20/EC of the European Parliament and of the… (LawPlayer, data as of 2026-07-04)
© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.
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