The Human Medicines Regulations 2012, Paragraph 62 is up to date with all changes known to be in force on or before 10 March 2025. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
62. In Schedule 7 (standard provisions for manufacturing authorisations)—U.K.
(a)in Part 2—
(i)in paragraph 5 for “the Act” substitute “ the 2012 Regulations ”,
(ii)in paragraph 9 for “the Act or any regulations under the Act” substitute “ or the 2012 Regulations ”, and
(iii)in paragraph 13—
(aa)for “Part II of the Act” substitute “ Parts 3 to 8 of the 2012 Regulations ”, and
(bb)for “the Act” in the second place where it occurs substitute “ the 2012 Regulations ”; and
(b)in Part 3—
(i)in paragraph 6 for “the Act” in the first place where it occurs substitute “ the 2012 Regulations ”, and
(ii)in paragraph 8—
(aa)for “Part II of the Act” substitute “ Parts 3 to 8 of the 2012 Regulations ”, and
(bb)for “the Act” in the second place where it occurs substitute “ the 2012 Regulations ”.
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