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  2. Food and Drugs Act - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drugs_Act

    The Food and Drugs Act (French: Loi sur les aliments et drogues) is an act of the Parliament of Canada regarding the production, import, export, transport across provinces and sale of food, drugs, contraceptive devices and cosmetics (including personal cleaning products such as soap and toothpaste). It was first passed in 1920 and most recently ...

  3. Health in Italy - Wikipedia

    en.wikipedia.org/wiki/Health_in_Italy

    [7] [8] As with any developed country, Italy has adequate and sufficient water and food distribution, and levels of nutrition and sanitation are high. In Italy, medical care is provided for free under a universal healthcare system, which operates on the assumption that healthcare is a human right and should be accessible to everyone regardless ...

  4. 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 ...

  5. Regulation of therapeutic goods - Wikipedia

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

    In Canada, regulation of therapeutic goods is done by Health Canada and governed by the Food and Drug Act and associated regulations. In addition, the Controlled Drugs and Substances Act specifies additional regulatory requirements for controlled drugs and drug precursors. [18]

  6. Italy looks to foreigners for quick fix to sickly health service

    www.aol.com/news/italy-looks-foreigners-quick...

    Highlighting the strains facing health services in Italy, the southern region of Calabria has signed a three-year deal to draft in almost 500 medics from the Caribbean island to help overcome a ...

  7. Health Products and Food Branch - Wikipedia

    en.wikipedia.org/wiki/Health_Products_and_Food...

    The EUND pathway was developed to allow a mechanism for authorization of these drugs based on non-clinical and limited clinical information. A manufacturer of a new drug may file an extraordinary use new drug submission for the new drug if, under paragraph C.08.002.01(1): [2] (a) the new drug is intended for

  8. Therapeutic Products Directorate - Wikipedia

    en.wikipedia.org/wiki/Therapeutic_Products...

    Prior to being given market authorization, a manufacturer must present substantive scientific evidence of a product's safety, efficacy, and quality as required by the Food and Drugs Act and Regulations. [1] It is one of the ten operational directorates of the Health Products and Food Branch, a branch of Health Canada.

  9. Assessing Claims About a Supposed Investigation Into the ...

    www.aol.com/news/assessing-claims-supposed...

    Bergamo—a city close to Milan in Italy’s northern Lombardy region—was home to the West’s first significant, and potentially most deadly, COVID-19 outbreak in early 2020.