# The Human Medicines Regulations 2012, Paragraph 33


Where and in so far as the licence relates to special medicinal products, the licence holder may only import such products from , in the case of an import into Great Britain, an approved country for import and in the case of an import into Northern Ireland, an EEA State—
(a) in response to an order which satisfies the requirements of regulation 167, and
(b) where the conditions set out in paragraphs 34 to 41 are complied with.

---
Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/33 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-33
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.