- Deddfwriaeth Ddrafft
This is a draft item of legislation. This draft has since been made as a UK Statutory Instrument: The Human Medicines (Amendment etc.) (EU Exit) Regulations 2020 No. 1488
167. For regulation 211 (amendment of regulation 279 (products without a marketing authorisation)) substitute—
“211. For regulation 279 substitute—
“279.—(1) A person may not publish an advertisement in Great Britain for a medicinal product unless one of the following is in force for the product—
(a)a UKMA(GB) or UKMA(UK);
(b)a COR(GB) or COR(UK); or
(c)a THR(GB) or THR(UK).
(2) A person may not publish an advertisement in Northern Ireland for a medicinal product unless one of the following is in force for the product—
(a)a UKMA(NI) or UKMA(UK);
(b)a COR(NI) or COR(UK);
(c)a THR(NI) or THR(UK);
(d)an EU marketing authorisation; or
(e)an Article 126a authorisation.
(3) A person may not publish an advertisement in the whole United Kingdom for a medicinal product unless, in relation to that product—
(a)one of the authorisations or registrations specified in paragraph (1) is in force in Great Britain; and
(b)one of the authorisations or registrations specified in paragraph (2) is in force in Northern Ireland.”.”.
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Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
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