The Medicines for Human Use (Clinical Trials) (Amendment) Regulations 2025
Write the words of this act the way you think they should read. Solon shows your change as a redline against the published text and pins it to that exact text, so it can never be applied to wording you did not see.
Change 1
30 Amendment to regulation 43
(1) Regulation 43 (qualified persons) is amended as follows. (2) In paragraph (2A)(b), for “Article 13 of the Directive” substitute “Article 62 of the EU Regulation”. (3) In paragraph (2C)(b), after “Commission Directive 2003/94/EC” insert “in respect of Great Britain or Commission Delegated Regulation 2017/1569 in respect of Northern Ireland”. (4) In paragraph (5), for “the said Article 49 or 50” substitute “Schedule 7 to the 2012 Regulations”. (5) In paragraph (6)(a)(i), for “the said Articles 49 or 50 of Directive 2001/83/EC” substitute “Schedule 7 to the 2012 Regulations”.
30 Amendment to regulation 43
(1) Regulation 43 (qualified persons) is amended as follows. (2) In paragraph (2A)(b), for “Article 13 of the Directive” substitute “Article 62 of the EU Regulation”. (3) In paragraph (2C)(b), after “Commission Directive 2003/94/EC” insert “in respect of Great Britain or Commission Delegated Regulation 2017/1569 in respect of Northern Ireland”. (4) In paragraph (5), for “the said Article 49 or 50” substitute “Schedule 7 to the 2012 Regulations”. (5) In paragraph (6)(a)(i), for “the said Articles 49 or 50 of Directive 2001/83/EC” substitute “Schedule 7 to the 2012 Regulations”.
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