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  2. List of European Union directives - Wikipedia

    en.wikipedia.org/wiki/List_of_European_Union...

    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 ...

  3. Human Medicines (Coronavirus and Influenza) (Amendment ...

    en.wikipedia.org/wiki/Human_Medicines...

    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 ...

  4. List of COVID-19 pandemic legislation - Wikipedia

    en.wikipedia.org/wiki/List_of_COVID-19_pandemic...

    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

  5. European Union response to the COVID-19 pandemic - Wikipedia

    en.wikipedia.org/wiki/European_Union_response_to...

    Some EU agencies are involved in the European Union response to the COVID-19 pandemic. [ 26 ] For instance, the European Medicines Agency (EMA), located in Amsterdam, is involved in providing information about the coronavirus pandemic, expediting the development and approval of safe and effective treatments and vaccines, and supporting the ...

  6. Human Medicines Regulations 2012 - Wikipedia

    en.wikipedia.org/wiki/Human_Medicines...

    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 The regulations partially repealed the Medicines Act 1968 in line with EU ...

  7. File:EUR 2018-1139.pdf - Wikipedia

    en.wikipedia.org/wiki/File:EUR_2018-1139.pdf

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  8. EU could approve shot against new coronavirus variant in 3-4 ...

    www.aol.com/news/eu-drug-watchdog-chief-could...

    (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 ...

  9. European Medicines Agency - Wikipedia

    en.wikipedia.org/wiki/European_Medicines_Agency

    According to EU Law the European Commission had to decide on the fate of the EMA's location. The EU ministers met to vote on their preferred successor. [ 28 ] The EU's Health Commissioner Vytenis Andriukaitis said that the preferred choice would be a location where an "easy set up and guarantee of smooth operations" would be available.