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Commission Directive 66/683/EEC of 7 November 1966 eliminating all differences between the treatment of national products and that of products which, under Articles 9 and 10 of the Treaty, must be admitted for free movement, as regards laws, regulations or administrative provisions prohibiting the use of the said products and prescribing the use of national products or making such use subject ...
Health Protection (Coronavirus, International Travel) (England) Regulations 2020 The Health Protection (Coronavirus, Restrictions) (Self-Isolation) (England) Regulations 2020 First COVID-19 tier regulations in England
The European Union drug regulator said Thursday it has started a rolling review of a new coronavirus vaccine made by French startup Valneva, the first step toward giving the vaccine the green ...
(Reuters) -The EU drug regulator said on Tuesday it could approve vaccines adapted to target the Omicron variant of the coronavirus within three to four months if needed, but that existing shots ...
EUDCC QR code displayed on a smartphone Sample EU Digital COVID Certificate issued by the Czech Republic. The EU Digital COVID Certificate (EUDCC), best known in Italy as the Green Pass and in France as the Sanitary Pass or Health Pass (passe sanitaire), was a digital certificate that a person has been vaccinated against COVID-19, tested for infection with SARS-CoV-2, or recovered from COVID ...
The European Medicines Agency (EMA) operates as a decentralised scientific agency (as opposed to a regulatory authority) of the European Union (EU) and its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. [8]
The Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2020 (SI 2020/1125) is a statutory instrument (SI) that was laid before Parliament on 16 October 2020 to make provision for the strengthening of existing regulations that allow for the temporary authorisation of the supply of unlicensed medicines, including vaccines, in response to certain public health threats, and for ...
The Human Medicines Regulations 2012 in the United Kingdom were created, under statutory authority of the European Communities Act 1972 and the Medicines Act 1968 in 2012. The body responsible for their upkeep is the Medicines and Healthcare products Regulatory Agency. The regulations partially repealed the Medicines Act 1968 in line with EU ...
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related to: eu regulations and directives on coronavirus vaccine