The Human Medicines Regulations 2012

[F1Obligation on licensing authority to maintain list of medicinal products to which derogations have appliedU.K.

This section has no associated Explanatory Memorandum

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.]

Textual Amendments