# Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, Division 7.2

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

Devices for self-testing must, where reasonably possible, include user control, i.e. a procedure by which the user can verify that, at the time of use, the product will perform as intended.

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Source: https://www.legislation.gov.uk/eudr/1998/79/annex/I/division/B/division/7/division/7.2 (the official version)
Page: https://openlegislation.uk/eu-directive-1998-79/annex-I/division-B/division-7/division-7.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.