- Draft legislation
This is a draft item of legislation. This draft has since been made as a UK Statutory Instrument: The Human Medicines (Amendments Relating to the Early Access to Medicines Scheme) Regulations 2022 No. 352
7. In regulation 43(6)(1) (obligations of licence holder), after sub-paragraph (a) insert—
“(aa)the supply, or offer for supply, of an unauthorised EAMS medicinal product in the United Kingdom;”.
Amended by S.I. 2016/186 and 2019/775.
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