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6. The standard provisions, for the purposes of Part II of the Act, for manufacturer’s licences, insofar as those licences relate to relevant medicinal products shall be—
(a)those provisions set out in Schedule 1, insofar as those licences relate to the manufacture and assembly of relevant medicinal products; and
(b)those provisions set out in Schedule 2, insofar as those licences relate to the import from a third country of relevant medicinal products.
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