# The Human Medicines Regulations 2012, Regulation 77: Record-keeping obligations

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

The holder of a marketing authorisation or parallel import licence must keep any documents or information that will facilitate the withdrawal or recall from sale or supply of any product to which the authorisation relates.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/77 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-77
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.