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Article 12
Member Sates shall appoint an adequate number of inspectors to ensure effective verification of compliance of clinical trials with applicable requirements, as well as the timely reporting of inspection findings.
Commission Implementing Regulation (EU) 2017/556 Article 12
Commission Implementing Regulation (EU) 2017/556 Article 12
Other provisions in CHAPTER III — INSPECTION PROCEDURES
- Article 6: Subject matter of inspections
- Article 7: Procedures to be established by Member States
- Article 8: Unannounced inspections
- Article 9: Collaboration between Member States
- Article 10: Powers of inspectors
- Article 11: Recognition of inspection conclusions
- Article 13: Inspection reports and records
- Article 14: Confidentiality
CitationArticle 12 of Commission Implementing Regulation (EU) 2017/556 (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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