# The Human Medicines Regulations 2012, Paragraph 62


In Schedule 7 (standard provisions for manufacturing authorisations)—
(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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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/34/paragraph/62 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-34/paragraph-62
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.