# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 2

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

The manufacturer must prepare the technical documentation described in section 3 and ensure that the manufacturing process follows the principles of quality assurance as set out in section 4.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/III/division/2 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-III/division-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.