Parallel import licencesU.K.
172.—(1) The prohibitions in regulation 46 (requirement for authorisation) do not prevent—
(a)the holder of a parallel import licence from placing the medicinal product to which the licence relates on the market; or
(b)the sale or supply, or offer for sale or supply, of a medicinal product to which a parallel import licence relates, in accordance with the terms of that licence.
[F1(2) In this regulation “parallel import licence” has the same meaning as in regulation 48(2).]
Textual Amendments
F1Reg. 172(2) substituted (E.W.S.) (1.10.2014) by The Human Medicines (Amendment) (No. 2) Regulations 2014 (S.I. 2014/1878), regs. 1, 18 and reg. 172(2) substituted (N.I.) (1.10.2014) by The Human Medicines (Amendment) (No. 2) Regulations 2014 (S.R. 2014/324), regs. 1(1), 18