Regulation 3 Designation of the competent authority
United Kingdom
The Human Tissue Authority (in these Regulations referred to as “the Authority”) is designated F1, in relation to Northern Ireland, the competent authority for the purposes of F2the first, second, third and fourth Directives so far as they relate to tissue and cells.
Annotations
Textual amendments
- F1
Words in reg. 3 inserted (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(2) (as substituted by S.I. 2020/1306, regs. 1, 4); 2020 c. 1, Sch. 5 para. 1(1)
- F2
Words in reg. 3 substituted (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), 2(2)