# The Medical Devices (In Vitro Diagnostic Devices etc.) (Amendment) Regulations 2023, Regulation 3: Amendment to the Human Tissue Act 2004


In section 1 of the Human Tissue Act 2004 (authorisation of activities for scheduled purposes), in subsection (12), for paragraph (a), substitute—
“(a) the use of relevant material to the extent that such use is regulated by—
(i) the Medical Devices Regulations 2002 (S.I. 2002/618),
(ii) Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC, or
(iii) Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU, or”.

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Source: https://www.legislation.gov.uk/ukdsi/2023/9780348253696/regulation/3 (the official version)
Page: https://openlegislation.uk/draft-medical-devices-in-vitro-diagnostic-devices-etc-amendment-regulations-2023/regulation-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.