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  2. Title 21 of the Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Title_21_of_the_Code_of...

    Requirements for pasteurization of milk; Interstate shipment of turtles as pets. Interstate shipment of African rodents that may carry monkeypox. Sanitation on interstate conveyances (i.e. airplanes and ships) 1271 Requirements for human cells, tissues, and cellular and tissue-based products (i.e. the cGTPs).

  3. Mandatory labelling - Wikipedia

    en.wikipedia.org/wiki/Mandatory_labelling

    Mandatory labelling is mandated in most developed nations and increasingly also in developing nations, especially for food products, e.g. "Grade A" meats. With regard to food and drugs, mandatory labelling has been a major battleground between consumer advocates and corporations since the late 19th century.

  4. Marketing authorisation - Wikipedia

    en.wikipedia.org/wiki/Marketing_authorisation

    Depending on jurisdiction, the resulting document may be more detailed (in addition to data identifying the product and its marketing authorisation holder), for example containing addresses of all manufacturing sites, appended labelling, artwork of packaging components, etc. or may be simplified to a one-page document called certificate of ...

  5. Biologics license application - Wikipedia

    en.wikipedia.org/wiki/Biologics_License_Application

    A BLA is submitted by any legal person or entity who is engaged in manufacture or an applicant for a license who takes responsibility for compliance with product and establishment standards. Form 356h specifies the requirements for a BLA. This includes: Applicant information; Product/manufacturing information; Pre-clinical studies; Clinical studies

  6. Fair Packaging and Labeling Act - Wikipedia

    en.wikipedia.org/.../Fair_Packaging_and_Labeling_Act

    The Fair Packaging and Labeling Act is a U.S. law that applies to labels on many consumer products. It requires the label to state: The identity of the product; The name and place of business of the manufacturer, packer, or distributor; and; The net quantity of contents. The contents statement must include both metric and U.S. customary units.

  7. What to Know About the FDA’s New Definition of ... - AOL

    www.aol.com/know-fda-definition-healthy-foods...

    The U.S. Food and Drug Administration (FDA) announced a new definition of “healthy” food for the first time in 30 years. The new definition will apply to manufacturers who want to call their ...

  8. Mandatory country-of-origin labeling (US) - Wikipedia

    en.wikipedia.org/wiki/Mandatory_country-of...

    The product is no longer identifiable as shrimp but as "quiche." The quiche is a product of the US. So labeling it as "product of the USA" would not be a violation of the FFD&C Act. (Whether or not it violates *CBP's* requirements would need to be asked.) An imported product, such as shrimp, is peeled and deveined.

  9. List of food labeling regulations - Wikipedia

    en.wikipedia.org/wiki/List_of_food_labeling...

    Regulation 1151/2012 on quality schemes for agricultural products and foodstuffs: defines "labelling" as "any words, particulars, trade marks, brand name, pictorial matter or symbol relating to a foodstuff and placed on any packaging, document, notice, label, ring or collar accompanying or referring to such foodstuff". [10]