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  2. Marketed Health Products Directorate - Wikipedia

    en.wikipedia.org/wiki/Marketed_Health_Products...

    The Marketed Health Products Directorate (MHPD) is the Canadian federal authority that monitors the safety and effectiveness of health products marketed in Canada. These include: [1] Prescription and non-prescription medications; Biologic medical products, including fractionated blood products; Therapeutic and diagnostic vaccines; Natural ...

  3. Food labelling in Canada - Wikipedia

    en.wikipedia.org/wiki/Food_labelling_in_Canada

    Unless otherwise exempted, pre-packaged [9] multi-ingredient foods require by law, an ingredient list. [10] In Canada, the ingredients must be displayed in both English and French unless exempted. Ingredients and their components (ingredients of ingredients) also must be listed under their specific names; [ 7 ] for example, whey protein must be ...

  4. 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 ...

  5. Health Canada - Wikipedia

    en.wikipedia.org/wiki/Health_Canada

    Health Canada (HC; French: Santé Canada, SC) [NB 1] is the department of the Government of Canada responsible for national health policy. The department itself is also responsible for numerous federal health-related agencies, including the Canadian Food Inspection Agency (CFIA) and the Public Health Agency of Canada (PHAC), among others.

  6. Health Products and Food Branch - Wikipedia

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

    (b) the requirements set out in paragraphs C.08.002(2)(g) and (h) cannot be met because (i) exposing human volunteers to the substance referred to in paragraph (a) would be potentially lethal or permanently disabling, and (ii) the circumstances in which exposure to the substance occurs are sporadic and infrequent.

  7. Medical food - Wikipedia

    en.wikipedia.org/wiki/Medical_food

    Medical foods are regulated by the US Food and Drug Administration under the Food Drug and Cosmetic Act regulations. 21 CFR 101.9(j) (8). [1]The term medical food, as defined in section 5(b) of the Orphan Drug Act (21 U.S.C. 360ee (b) (3)) is "a food which is formulated to be consumed or administered enterally under the supervision of a physician and which is intended for the specific dietary ...

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    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Category:Regulation of medical devices - Wikipedia

    en.wikipedia.org/wiki/Category:Regulation_of...

    Medical Devices regulations cover all the topics related to the laws, standards or submissions process, with which compliance is required by manifold national and international bodies to commercialize a medical device