enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Regulation and prevalence of homeopathy - Wikipedia

    en.wikipedia.org/wiki/Regulation_and_prevalence...

    The FDA held a hearing April 20 and 21, 2015, requesting public comment on regulation of homeopathic drugs. [80] Citing the growth of sales of over-the-counter homeopathic medicines, $2.7 billion as of 2007, many labeled as "natural, safe, and effective", the FDA asked: [81]

  3. Homeopathy - Wikipedia

    en.wikipedia.org/wiki/Homeopathy

    In some countries, there are no specific legal regulations concerning the use of homeopathy, while in others, licences or degrees in conventional medicine from accredited universities are required. In 2001 homeopathy had been integrated into the national health care systems of many countries, including India, Mexico, Pakistan, Sri Lanka, and ...

  4. European Directive on Traditional Herbal Medicinal Products

    en.wikipedia.org/wiki/European_Directive_on...

    The European Directive on Traditional Herbal Medicinal Products (THMPD), formally the Directive 2004/24/EC amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use, was established by the European Parliament and Council on 31 March 2004 to provide a simplified regulatory approval process for traditional ...

  5. Medicines and Healthcare products Regulatory Agency

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

    The MHRA has several independent advisory committees which provide the UK Government with information and guidance on the regulation of medicines and medical devices. There are currently eight such committees: [citation needed] Advisory Board on the Registration of Homeopathic Products; Herbal Medicines Advisory Committee; The Review Panel

  6. Regulation of alternative medicine - Wikipedia

    en.wikipedia.org/wiki/Regulation_of_alternative...

    Regulation of medicines and medical devices, to ensure they work and are acceptably safe, is the responsibility of the Medicines and Healthcare products Regulatory Agency. The legal status of medicines is determined under the Medicines Act 1968 and European Council Directive 2001/83/EC which control the sale and supply of medicines.

  7. Federal Food, Drug, and Cosmetic Act of 1938 - Wikipedia

    en.wikipedia.org/wiki/Federal_Food,_Drug,_and...

    Medical Device Regulation Act, PL 94–295, 90 Stat 539; Radiation Control for Health and Safety Act of 1968, PL 90-602, 82 Stat 1173; Drug Price Competition and Patent Term Restoration Act of 1984, PL 98-471, 98 Stat 1585; Nutrition Labeling and Education Act (1990), PL 101-535, 104 Stat 2353

  8. Homeopathic dilutions - Wikipedia

    en.wikipedia.org/wiki/Homeopathic_dilutions

    Even though the homeopathic preparations are often extremely diluted, homeopaths maintain that a healing force is retained by these homeopathic preparations. [34] Modern advocates of homeopathy have proposed a concept of " water memory ", according to which water "remembers" the substances mixed in it, and transmits the effect of those ...

  9. Natural health product - Wikipedia

    en.wikipedia.org/wiki/Natural_health_product

    Under the regulations, all natural health products require a Natural Product Number (NPN), analogous to the Drug Identification Numbers (DINs) used to identify and monitor drugs in Canada. Natural Health Products are defined in Canada as: Vitamins and minerals [5] Salt of Székely Land, 2014; Herbal remedies; Homeopathic medicines