Commission Implementing Regulation (EU) 2023/1020 of 24 May 2023 amending Regulation (EU) No 965/2012 as regards helicopter emergency medical service operations
Edition 2023-05-24

Commission Implementing Regulation (EU) 2023/2713 of 5 December 2023 designating European Union reference laboratories in the field of in vitro diagnostic medical devices
Edition 2023-12-05

Commission Recommendation of 5 April 2013 on a common framework for a unique device identification system of medical devices in the Union
Edition 2013-04-05

COUNCIL DIRECTIVE 92/29/EEC of 31 March 1992 on the minimum safety and health requirements for improved medical treatment on board vessels
Edition 1992-03-31

Commission Recommendation (EU) 2024/1112 of 18 April 2024 on clinical audits of medical radiological practices carried out pursuant to Council Directive 2013/59/Euratom
Edition 2024-04-18

Commission Recommendation of 24 September 2013 on the audits and assessments performed by notified bodies in the field of medical devices
Edition 2013-09-24

Council Regulation (EU) 2022/2372 of 24 October 2022 on a framework of measures for ensuring the supply of crisis-relevant medical countermeasures in the event of a public health emergency at Union level
Edition 2022-10-24

Commission Regulation (EU) 2023/2482 of 13 November 2023 amending Regulation (EC) No 1907/2006 of the European Parliament and of the Council as regards the substance bis(2-ethylhexyl) phthalate (DEHP) in medical devices
Edition 2023-11-13

Commission Directive 2014/82/EU of 24 June 2014 amending Directive 2007/59/EC of the European Parliament and of the Council as regards general professional knowledge and medical and licence requirements
Edition 2014-06-24

Commission Implementing Decision (EU) 2024/581 of 16 February 2024 on the harmonised standard for accreditation of medical laboratories drafted in support of Regulation (EC) No 765/2008 of the European Parliament and of the Council
Edition 2024-02-16