# Council Directive of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices (90/385/EEC), Division 2.3.6

Extent: E+W+S+N.I.

The investigations shall be performed under the responsibility of an duly qualified medical practitioner or authorised person, in an appropriate environment.
The medical specialist shall have access to the technical data regarding the device.

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Source: https://www.legislation.gov.uk/eudr/1990/385/annex/7/division/2/division/2.3/division/2.3.6 (the official version)
Page: https://openlegislation.uk/eu-directive-1990-385/annex-7/division-2/division-2.3/division-2.3.6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.