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5. After regulation 345 insert—
345A.—(1) The licensing authority must publish a list of medicinal products to which the derogations described in Articles 5a, 8(2a) and (2b), 18a, 20 (second paragraph), 40(1a) and (3a), 48(3) and 104(3) of the 2001 Directive have applied.
(2) The licensing authority must update the list referred to in paragraph (1) at least every six months.”.
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