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2. File:Medicines Act 1968 (UKPGA 1968-67 qp).pdf - Wikipedia

   en.wikipedia.org/wiki/File:Medicines_Act_1968...

   English: An Act to make new provision with respect to medicinal products and related matters, and for purposes connected therewith. Publication date 25 October 1968

3. Medicines Act 1968 - Wikipedia

   en.wikipedia.org/wiki/Medicines_Act_1968

   The act defines three categories of medicine: prescription only medicines (POM), [3] which are available only from a pharmacist if prescribed by an appropriate practitioner (including, but not limited to doctors, dentists, optometrists, prescribing pharmacists and nurses); pharmacy medicines (P), available only from a pharmacist but without a ...

4. File:Health and Medicines Act 1988 (UKPGA 1988-49).pdf ...

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

   About Wikipedia; Contact us; ... Health and Medicines Act 1988 (UKPGA 1988-49).pdf ... Page contents not supported in other languages. File; Talk; English. Read; View ...

5. File:Medicines Act 1971 (UKPGA 1971-69 qp).pdf - Wikipedia

   en.wikipedia.org/wiki/File:Medicines_Act_1971...

   About Wikipedia; Contact us; ... Medicines Act 1971 (UKPGA 1971-69 qp).pdf ... Page contents not supported in other languages. File; Talk; English. Read; View on Commons;

6. Affordable Care Act - Wikipedia

   en.wikipedia.org/wiki/Affordable_Care_Act

   The Affordable Care Act (ACA), formally known as the Patient Protection and Affordable Care Act (PPACA) and informally as Obamacare, is a landmark U.S. federal statute enacted by the 111th United States Congress and signed into law by President Barack Obama on March 23, 2010.

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 The regulations partially repealed the Medicines Act 1968 in line with EU ...

8. Committee on Safety of Medicines - Wikipedia

   en.wikipedia.org/wiki/Committee_on_Safety_of...

   The Committee on Safety of Medicines (CSM) was an independent advisory committee that advised the UK Licensing Authority on the quality, efficacy, and safety of medicines. Following the thalidomide tragedy of 1957 to 1961, in 1963 the government asked Sir Derrick Dunlop to set up a committee to investigate the control and introduction of new ...

9. British Pharmacopoeia - Wikipedia

   en.wikipedia.org/wiki/British_Pharmacopoeia

   The British Pharmacopoeia is published on behalf of the Health Ministers of the United Kingdom; on the recommendation of the Commission on Human Medicines, in accordance with section 99(6) of the Medicines Act 1968, and notified in draft to the European Commission (EC) in accordance with Directive 98/34/EEC.