Paragraph 5A F1
United Kingdom
Where the Authority grants a licence under this Schedule authorising the carrying on of the activities to which regulation 7(1A) applies, it must provide the designated individual in relation to that licence with a F2certificate—
of authority in relation to Great Britain, in such form as the Authority considers appropriate,
in relation to Northern Ireland, in the form set out in Annex II to the fourth Directive.
Annotations
Textual amendments
- F1
Sch. 1 para. 5A inserted (6.3.2018 for specified purposes, 1.4.2018 in so far as not already in force) by The Human Tissue (Quality and Safety for Human Application) (Amendment) Regulations 2018 (S.I. 2018/335), regs. 1(2)(3), 7(2) (with reg. 10)
- F2
Words in Sch. 1 para. 5A 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(20) (as substituted by S.I. 2020/1306, regs. 1, 24); 2020 c. 1, Sch. 5 para. 1(1)