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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 ...
EUR-Lex is the official online database of European Union law and other public documents of the European Union (EU), published in 24 official languages of the EU. The Official Journal (OJ) of the European Union is also published on EUR-Lex. Users can access EUR-Lex free of charge and also register for a free account, which offers extra features.
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 ...
Problems with delivery thereof led to the European Commission–AstraZeneca COVID-19 vaccine dispute. [ citation needed ] On 1 December 2021, European Commission President Ursula von der Leyen said that EU nations should consider making COVID-19 vaccinations mandatory because too many people were refusing to get shots voluntarily.
Health Protection (Face Coverings in a Relevant Place) (England) Regulations 2020; 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; Second COVID-19 tier regulations in England
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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 The regulations partially repealed the Medicines Act 1968 in line with EU ...
The Directive 92/58/EEC specifies the minimum requirements for safety signs within the European Union. [1] It superseded the Directive 77/576/EEC. [1] While not being replaced by the standard ISO 7010, both signage systems can be used. [2] This directive does not apply to signage used for controlling roadway, railway, waterway or air ...