{"standard":"EN ISO 14155","listings":[{"edition":"EN ISO 14155:2011","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-medical-devices"},{"edition":"EN ISO 14155:2020","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Clinical investigation of medical devices for human subjects – Good clinical practice (ISO 14155:2020)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"}],"events":[{"date":"2026-01-30","type":"added","ref":"EN ISO 14155:2020","leg_slug":"mdr","leg_name":"Medical Devices Regulation"}],"generated":"2026-08-16 23:54 UTC"}