# The Human Medicines Regulations 2012, Regulation 257E: Regulation-making power as to certain forms of labelling


The Ministers may by regulations require the use of certain forms of labelling of a medicinal product in order to make it possible to ascertain—
(a) the price of the medicinal product;
(b) any reimbursement conditions of the National Health Service;
(c) the legal status for supply to the patient in accordance with regulation 5 (classification), insofar as not already provided for in Schedule 25;
(d) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/257E (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-257E
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.