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Animal Feed GRAS Notifications

Animal Feed GRAS Notifications

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Animal Feed GRAS Notifications

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  1. Animal Feed GRAS Notifications Geoffrey K. Wong, M.S. Division of Animal Feeds Center for Veterinary Medicine Pet Food Institute October 15, 2009

  2. Ingredient Safety Team • Geoff Wong, MS (Team Leader) • C. George Chang, DVM, PhD, DABT • Tom Hendricks, PhD, MPH • Marla Luther, PhD • Becky Muir, PhD

  3. GRAS Notification What is GRAS?!?

  4. What is GRAS? • GRAS – Generally Recognized As Safe • 1958 Food Additives Amendment to Federal Food, Drug and Cosmetic Act • Defined “food additive” • Required premarket approval of food additives • Established standards for safety and review • Created exemption to food additive definition • GRAS status for a specific use of substance

  5. GRAS Exemption • Any substance intentionally added to an animal feed must be used in accordance with a food additive regulation for that use unless the substance is GRAS among experts qualified by scientific training and experience to evaluate its safety under the conditions of its intended use

  6. GRAS Exemption (cont.) • What does this mean in practical terms? • General recognition of safety is for a substance for an intended use • Two points • Substances are not GRAS, it is a particular use of a substance that is GRAS • Feed use of substances varies with the animal species, thus • Feed GRAS determinations must address intended use in the intended animal species

  7. Food Additive vs. GRAS • Food additives require FDA premarket approval, a petition process • 21 CFR 571.1 • GRAS status is an exemption to food additive definition • FDA involvement is not required • Firms can do their own determination for whether requirements for GRAS status are met

  8. What Uses can be GRAS? • Food additive definition is very broad, but it does NOT include: • Pesticides • Color additives • Approved under another FDA premarket process • Drugs and new animal drugs • Some substances approved under specific laws administered by USDA • These substances cannot be GRAS

  9. GRAS Status • There are two parts to establish that a use of a substance is GRAS • Safety - Defined in 21 CFR 570.3(i) • General recognition - Addressed in 21 CFR 570.30 • Fair evaluation of the data… • Need to address all data and information • Cannot ignore the “inconvenient” or contradictory

  10. GRAS Status (cont.) • Safety – same as food additive Reasonable certainty of no harm • 21 CFR 570.3(i) lists factors to be considered • Consumption • Cumulative effect\exposure • Appropriate safety factors • For food animal species, need to consider possibility of tissue residues

  11. GRAS Status (cont.) • General Recognition • Information needed for GRAS determination • Must be generally available • Must be generally accepted by qualified experts • Information needed to establish GRAS status of an intended use of substance cannot be confidential

  12. Information • Generally available data and information • Usually means published studies • Can include information in text books • Availability allows review by any experts qualified by scientific experience and training to evaluate the safety of substances added to food • Consensus among experts about these data and information establishes GRAS status of intended use of substance

  13. Basis for GRAS Determinations Experts may base safety conclusions on: • Experience based on common use in animal food before 1958 • Data and information must be generally available • Need to show common use OR

  14. Basis for GRAS (cont.) • Scientific procedures • Most frequently used • Requires same quantity and quality of scientific evidence as required to obtain approval of a food additive regulation • Scientific evidence must be generally available GRAS status is more difficult to establish than a food additive regulation due to requirement for general recognition

  15. Safety Evaluations • Addressing animal safety is complex • Difficult to do cross-species comparisons of toxicity data • Recent NRC report found insufficient data to support extrapolation across species • Animal safety studies in the individual target species are often necessary • Human food safety may also need to be addressed, dependent on intended use

  16. GRAS Notification • Proposed rule published in 1997 • Changing from petition to notification process • Publication date of final rule is unclear • CVM implementing pilot program • Resources are still an issue • Will be announced in the Federal Register • Anticipated start date • Late 2009

  17. GRAS Notification (cont.) • Pilot program based on 1997 proposal • Voluntary • Firms can conduct a GRAS determination without notifying FDA • Notice informs FDA of notifier’s determination that a use of a substance is GRAS • Notifier’s determination and responsibility • Summary document, not raw data/complete reports • FDA responds by letter • Notifier can withdraw notice at any time, stops FDA review

  18. Highlights of Notice • Talk to CVM as putting notice together • Summary of notifier’s determination • GRAS notice should include: • Statement of GRAS determination • Detailed information about identity of substance • Chemical identification • Method of manufacture, exclude trade secret information • Source of substance • Characteristic properties • Specifications • Utility – Intended Uses, Levels, Target Animal Species

  19. Highlights of Notice (cont.) • Comprehensive discussion of basis for GRAS determination • Consideration of Food and Water Exposure • Safety – reasonable certainty of no harm • Animal and, potentially human food, safety • Favorable and unfavorable data/information • Basis for GRAS status in light of both favorable and unfavorable information - fair evaluation • Other administrative information

  20. Types of FDA Response • No questions • Based on the information provided by [notifier], … the agency has no questions at this time regarding [notifier’s conclusion that [substance] is GRAS under the intended conditions of use. The agency has not, however, made its own determination regarding … GRAS status • No basis • FDA has evaluated the information in [the GRAS Notice]…as well as other available data and information. Your notice does not provide a sufficient basis for a determination that [substance] is GRAS under the conditions of its intended use.

  21. GRAS Notification (cont.) • Inventory of GRAS notices and FDA responses on the Internet • Notices available under Freedom of Information Act (FOIA) • May also be posted on Internet • General recognition means information that establishes safety cannot be confidential • CVM’s process will be similar to CFSAN’s on-going pilot program • Information about CFSAN pilot program at

  22. Questions?

  23. C V M enter for eterinary edicine Thank You