# The Medical Devices (Amendment) Regulations 2008, Regulation 13: Amendment of regulation 29 of the principal Regulations


In regulation 29 of the principal Regulations (procedures for active implantable medical devices for clinical investigations), after paragraph (9) add—
“(10) The manufacturer, or their single authorised representative, shall—
(a) notify the Secretary of State of the end of the clinical investigation; and
(b) provide justification where premature termination has resulted.”.

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Source: https://www.legislation.gov.uk/uksi/2008/2936/regulation/13 (the official version)
Page: https://openlegislation.uk/medical-devices-amendment-regulations-2008/regulation-13
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.