# Medicines Act 1968, Section 67E: Sections 67A to 67D: “adulteration” and “registrant”


In sections 67A to 67D—
“adulteration”, in relation to a medicinal product, means the addition of a substance to, or the abstraction of a substance from, the product, so as to affect injuriously its composition (and related expressions are to be construed accordingly);
“registrant” means—
(a)where it is alleged that the offence in question took place in Great Britain, a person who is entered in Part 1, or 2 of the register of pharmacists and pharmacy technicians established and maintained under article 19 of the Pharmacy Order 2010 (SI 2010/231); or
(b)where it is alleged that the offence in question took place in Northern Ireland, a person registered in the register of pharmaceutical chemists for Northern Ireland ... maintained under articles 6 and 9 of the Pharmacy (Northern Ireland) Order 1976 (SI 1976/1213 (NI 22)).

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Source: https://www.legislation.gov.uk/ukpga/1968/67/section/67E (the official version)
Page: https://openlegislation.uk/medicines-act-1968/section-67E
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.