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  2. Medicines and Healthcare products Regulatory Agency

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

    The MHRA and the US Food and Drug Administration were criticised in the 2012 book Bad Pharma, [43] and in 2004 by David Healy in evidence to the House of Commons Health Committee, [44] for having undergone regulatory capture, i.e. advancing the interests of the drug companies rather than the interests of the public.

  3. Clinical Practice Research Datalink - Wikipedia

    en.wikipedia.org/wiki/Clinical_Practice_Research...

    The Clinical Practice Research Datalink (CPRD) is an observational and interventional research service that operates as part of the Department of Health and Social Care.It is jointly funded by the National Institute for Health and Care Research (NIHR) and the Medicines and Healthcare products Regulatory Agency (MHRA).

  4. Baby Doe Law - Wikipedia

    en.wikipedia.org/wiki/Baby_Doe_Law

    The HHS also obtained copies of the infant's medical records for her first week of life, which were reviewed by Koop, who stated that he did not see anything in the record that would exclude the child from surgery. [5] HHS took the stance that Baby Jane Doe was being discriminated against due to her medical conditions and mental disability.

  5. Commission on Human Medicines - Wikipedia

    en.wikipedia.org/wiki/Commission_on_Human_Medicines

    The Commission on Human Medicines (CHM) is a committee of the UK's Medicines and Healthcare products Regulatory Agency.It was formed in October 2005, and assumed the responsibilities of the Medicines Commission and the Committee on Safety of Medicines.

  6. Therapeutic privilege - Wikipedia

    en.wikipedia.org/wiki/Therapeutic_privilege

    Examples given by the court included geriatric patients and those with anxiety disorders, whose state of mind may prohibit understanding the true reality of low-risk treatments which are safe and provide an advantage to the patient and therefore therapeutic privilege should 'extend to cases where although patients have mental capacity, their ...

  7. 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 ...

  8. List of mental disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_mental_disorders

    This is an accepted version of this page This is the latest accepted revision, reviewed on 17 February 2025. The following is a list of mental disorders as defined at any point by the Diagnostic and Statistical Manual of Mental Disorders (DSM) or the International Classification of Diseases (ICD). A mental disorder, also known as a mental illness, mental health condition, or psychiatric ...

  9. Prevention of mental disorders - Wikipedia

    en.wikipedia.org/wiki/Prevention_of_mental_disorders

    using preventive strategies particularly for children at risk (such as children of parents with mental illness, or with family stresses such as divorce or job loss). [78] In India the 1982 National Mental health Programme included prevention, [79] but implementation has been slow, particularly of prevention elements. [80] [81] [82]