The Human Medicines Regulations 2012

[F1Regulation-making power as to certain forms of labellingU.K.
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257E.  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;

F2(d). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .]

Textual Amendments