165. Nothing in this Part prevents the licensing authority from determining that a product is a medicinal product [F1in relation to these Regulations] without following the procedures in this Part when it thinks it appropriate.
Textual Amendments
F1Words in reg. 165 inserted (E.W.S.) (31.3.2014) by The Human Medicines (Amendment) Regulations 2014 (S.I. 2014/490), regs. 1(2), 3 and words in reg. 165 inserted (N.I.) (31.3.2014) by The Human Medicines (Amendment) Regulations 2014 (S.R. 2014/323), regs. 1(2), 3