# The Human Medicines (Amendment) Regulations 2019, Regulation 19: Amendment of Schedule 24 (packaging information requirements)


In schedule 24, after paragraph 18 insert—
“18A. In the case of a medicinal product, other than a radiopharmaceutical, that is required by Article 54a of the 2001 Directive to bear safety features—
(a) a unique identifier which complies with the technical specifications set out in Chapter II of Commission Regulation 2016/161; and
(b) an anti-tampering device allowing verification of whether the packaging of the medicinal product has been tampered with.”.

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Source: https://www.legislation.gov.uk/uksi/2019/62/regulation/19 (the official version)
Page: https://openlegislation.uk/human-medicines-amendment-regulations-2019/regulation-19
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.