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Public Meeting New Dietary Ingredient Program

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Director, Division of Dietary Supplement Programs. Office of Nutritional Products, Labeling, and Dietary Supplements. Lead Scientist for Dietary Supplement Safety ... – PowerPoint PPT presentation

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Title: Public Meeting New Dietary Ingredient Program


1
Public MeetingNew Dietary Ingredient Program
  • November 15, 2004
  • Susan J. Walker, M.D.
  • Director, Division of Dietary Supplement Programs
  • Office of Nutritional Products, Labeling, and
    Dietary Supplements
  • Lead Scientist for Dietary Supplement Safety
  • Center for Food Safety and Applied Nutrition

2
FDA/CFSAN/ONPLDS
  • Division of Dietary Supplement Programs
  • Branches/Teams
  • Compliance - Robert Moore, Ph.D.
  • Regulations and Review - Linda Pellicore, Ph.D.
  • Clinical Evaluation - Jason Woo, M.D.
  • Special Assistant for Science Review
  • Vasilios Frankos, Ph.D.

3
Additional Panel Members
  • Michael Landa,
  • Deputy Director for Regulatory Affairs
  • Barbara Schneeman, PhD
  • Director, ONPLDS
  • Jeanne Rader, PhD
  • Director, Division of Research Applied Technology
  • Alan Rulis, PhD
  • Senior Advisor for Special Projects

4
75 day New Dietary Ingredient Notifications
Dietary substances or constituents, etc.
Botanical extracts
Botanicals (whole,dried, ground, etc)
Vitamins, minerals and amino acids ?
5
Concerns with Notifications
  • Failure to
  • Describe the new dietary ingredient
  • Show why it is a new dietary ingredient
  • Provide adequate safety information
  • Provide other necessary information
  • Notifications and FDA responses publicly
    available in dockets

6
75 Day Notifications - Outcomes
7
Is the substance an eligible dietary
ingredient Section 201(ff) (1), (2), (3)
Was the dietary Ingredient marketed in the US
prior to October 15, 1994?
Yes
No
New Dietary Ingredient Section 413 (c)
Not New Dietary Ingredient
8
New Dietary Ingredient
Has the ingredient been present in food supply
as article used for food not chemically altered
No
Notify FDA (75 day NDI requirement)
Does there exist a history of use or other
safety evidence for DS
Adulteration provision
9
Scope of Meeting
  • Status of substance as a new dietary ingredient
  • Chemical identification of the NDI
  • Information about the dietary supplement

10
Scope of Meeting
  • Establishing a reasonable expectation of safety
  • Role of definitions in evaluating new dietary
    ingredients
  • Is there a need for guidance or amendment of
    current requirements?
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