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Commission Implementing Regulation (EU) 2017/556 Article 9

Commission Implementing Regulation (EU) 2017/556 Article 9

Collaboration between Member States

Article 9

1.   Member States shall collaborate with each other, with the Commission and with the European Medicines Agency to develop and improve commonly recognised standards of good clinical practice inspections. This collaboration may take the form of joint inspections, agreed processes and procedures and sharing of experience and training. 2.   The Commission shall make publicly available any guidance documents on the commonly recognised standards for the conduct of inspections, developed in collaboration with Member States and the European Medicines Agency. 3.   The European Medicines Agency shall process and make available to Member States information on inspections that are envisaged, scheduled, or conducted, in order to assist Member States to ensure the most efficient use of inspection resources when planning their inspections. 4.   Member States may request assistance from the national competent authority of another Member State in the matter of inspection.

Read the full instrument → · Read this in context: CHAPTER III — INSPECTION PROCEDURES →

Other provisions in CHAPTER III — INSPECTION PROCEDURES

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 9 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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