This section has no associated Explanatory Memorandum
[F11. In relation to Great Britain, directions shall require that licence holders adopt such systems as the Authority considers appropriate to secure, in relation to traceability, compliance with the requirements of Article 8 of the first Directive (traceability) and Article 9 of the third Directive (traceability).]U.K.
Textual Amendments
F1Sch. 2 para. 1 substituted (31.12.2020) by The Human Tissue (Quality and Safety for Human Application) (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/481), regs. 1, 3(21)(a) (as amended by S.I. 2020/1306, regs. 1, 25(a)); 2020 c. 1, Sch. 5 para. 1(1)