Adaptation to scientific and technical progress
Article 20
This Directive shall be adapted to take account of scientific and technical progress in accordance with the procedure referred to in Article 21(2).
Directive 2001/20/EC of the European Parliament and of the… Article 20
Directive 2001/20/EC of the European Parliament and of the… Article 20
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 21: Committee procedure
- Article 22: Application
- Article 23: Entry into force
- Article 24: Addressees
CitationArticle 20 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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