# The Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994, Paragraph 2: Introductory


The requirements of this Schedule supplement those of Council Directive 92/27/EEC relating to:
(a) special warnings necessary for particular medicinal products;
(b) the legal status for supply to the patient, in accordance with Council Directive 92/26/EEC;
(c) identification and authenticity.

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Source: https://www.legislation.gov.uk/uksi/1994/3144/schedule/5/paragraph/2 (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-marketing-authorisations-etc-regulations-1994/schedule-5/paragraph-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.