Search results
Results from the WOW.Com Content Network
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file
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 ...
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 ...
The main types of acts under this heading are EU treaties (sector 1), directives, regulations, decisions as well as consolidated legislation (sector 0), etc. Consolidation is the integration of a basic legal act and all of its successive amendments and corrigenda into one easy-to-read document. Consolidated texts are intended for use as ...
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
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 The regulations partially repealed the Medicines Act 1968 in line with EU ...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 date by which the Regulation was to be fully implemented by replacing the previous directives was originally defined as 26 May 2020. Following the international health emergency COVID-19, the European Commission and the European Parliament decided in April 2020 to postpone the deadline by one year to 26 May 2021. [10]
The L series (= Legislation) contains EU legislation including regulations, directives, decisions, recommendations, and opinions. The C series (= Courts) contains reports and announcements, including the judgments of the European Court of Justice and the General Court (formerly known as the Court of First Instance).