http://www.legislation.gov.uk/eur/2017/556/article/7Commission Implementing Regulation (EU) 2017/556 of 24 March 2017 on the detailed arrangements for the good clinical practice inspection procedures pursuant to Regulation (EU) No 536/2014 of the European Parliament and of the Council (Text with EEA relevance)Commission Implementing Regulation (EU) 2017/556Commission Implementing Regulation (EU) 2017/556 of 24 March 2017 on the detailed arrangements for the good clinical practice inspection procedures pursuant to Regulation (EU) No 536/2014 of the European Parliament and of the Council (Text with EEA relevance)2020-12-12King's Printer of Acts of Parliamenthttps://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32017R0556texttext/xmlen2017-03-24 CHAPTER III INSPECTION PROCEDURESProcedures to be established by Member States Article 7 1 Member States shall establish the relevant procedures for at least the following: a appointing experts to accompany inspectors, if additional expertise is required for an inspection; b arranging inspections outside the Union; c verification of good clinical practice compliance, including the modalities for examining the study management procedures and the conditions under which the clinical trial is planned, performed, monitored and recorded, as well as follow-up measures, such as a review of an analysis of the root cause of a significant non-compliance and verification of corrective and preventive actions implemented by the sponsor. Member States shall make those procedures and rules publicly available. 2 Member States shall also define the powers of experts appointed to accompany inspectors.