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2. Medicines and Healthcare products Regulatory Agency

   en.wikipedia.org/wiki/Medicines_and_Healthcare...

   The MHRA is funded by the Department of Health and Social Care for the regulation of medical devices, whilst the costs of medicines regulation is met through fees from the pharmaceutical industry. [6] This has led to suggestions by some MPs that the MHRA is too reliant on industry, and so not fully independent. [7]

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 The regulations partially repealed the Medicines Act 1968 in line with EU ...

4. Solid Converter PDF - Wikipedia

   en.wikipedia.org/wiki/Solid_Converter_PDF

   Solid Converter PDF is document reconstruction software from Solid Documents which converts PDF files to editable formats. Originally released for the Microsoft Windows operating system, a Mac OS X version was released in 2010. The current versions are Solid Converter PDF 9.0 for Windows and Solid PDF to Word for Mac 2.1.

5. List of stringent regulatory authorities - Wikipedia

   en.wikipedia.org/wiki/List_of_stringent...

   A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...

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

   en.wikipedia.org/wiki/Human_Medicines_(Corona...

   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 ...

7. MHRA - Wikipedia

   en.wikipedia.org/wiki/MHRA

   Download as PDF; Printable version; In other projects Wikidata item; ... MHRA may refer to: Organisations. Medicines and Healthcare products Regulatory Agency, UK;

8. File:The Medical Devices Regulations 2002 (UKSI 2002-618).pdf

   en.wikipedia.org/wiki/File:The_Medical_Devices...

   English: These Regulations contain the legislative measures necessary for the implementation of three European Community Directives- Council Directive 90-385-EEC on the approximation of the laws of the Member States relating to active implantable medical devices, as amended; Council Directive 93-42-EEC concerning medical devices, as amended; and Directive 98-79-EC of the European Parliament ...

9. Regulation of therapeutic goods - Wikipedia

   en.wikipedia.org/wiki/Regulation_of_therapeutic...

   The role of therapeutic goods regulation is designed mainly to protect the health and safety of the population. Regulation is aimed at ensuring the safety, quality, and efficacy of the therapeutic goods which are covered under the scope of the regulation. In most jurisdictions, therapeutic goods must be registered before they are allowed to be ...