Search Results for 'FDA'
Refine by Dates:
Refine By
Content Type
BlogBreaking News
Buyers Guide Companies
Classifieds
Columns
Consumer Trends
Editorials
Features
Health E-Insights
Industry Events
Industry News
Market Research
Monograph Center
Naturally Filtered
Online Exclusives
Patents
Peer-reviewed Research
People In The News
Products
Recent Certifications & Approvals
Suppliers Corner
Supplier Research
Supply Source
TrendSense
Webinars
Article Results
16 - 30 of 450 results
Published September 20, 2011
FDA has grossly underestimated the burden of its New Dietary Ingredient (NDI) notification process on the dietary supplement industry in terms of time resources, according to the Council for Responsible Nutrition (CRN), Washington, D.C., which submitted comments to the Office of Management and Budget. Read More »
Published September 8, 2011
Sabinsa Corporation, East Windsor, NJ, has received confirmation that five of its SAMI Labs in India (the company’s manufacturing center) recently underwent FDA inspection. FDA found no issues of concern in four of the facilities inspected. The… Read More »
Published September 8, 2011
FDA has extended the period to submit comments regarding the New Dietary Ingredient Notification Guidance by 60 days, to December 2, 2011.
Industry groups began calling for an extended comment period shortly after the agency issued… Read More »
By Todd Harrison
Published September 1, 2011
Discussing the highlights of the new guidance and what it means for the supplement business. Read More »
Published September 1, 2011
Trade associations respond, requesting an extended comment period. Read More »
Published September 1, 2011
Agency believes its proposed rule published in 2007 remains valid. Read More »
Published August 9, 2011
As awareness of gluten intolerance and sensitivity increases, FDA is looking to define “gluten-free” for labeling food products, including dietary supplements. Read More »
Published July 18, 2011
The Natural Products Association (NPA) held the dietary supplement industry’s first education session about the recently released New Dietary Ingredients (NDI) Draft Guidance by the Food and Drug Administration (FDA) on July 11. Read More »
By Todd Harrison, Claudia Lewis-Eng & Michelle Jackson
Published July 11, 2011
Discussing the highlights of the new guidance and what it means for the supplement business. Read More »
Published July 1, 2011
Florham Park, NJ-based Gerber Products Company, a part of the Nestlé family, has received notice from FDA that Gerber Good Start milk-based formulas meet the criteria for a qualified health claim related to a reduced risk of atopic dermatitis.… Read More »
Published May 26, 2011
Gerber Products Company, a part of the Nestlé family, has received notice from FDA that Gerber Good Start milk-based formulas meet the criteria for a qualified health claim related to a reduced risk of atopic dermatitis. Read More »
Published May 25, 2011
Natural Products Foundation (NPF) representatives met with Richard Cleland of the Federal Trade Commission (FTC) along with Gary Coody and others of the US Food and Drug Administration (FDA) on May 20th to present documentation regarding 13 non-compliant advertisers. Read More »
Published May 16, 2011
FDA has warned consumers about counterfeit products respresented as ExtenZe, a dietary supplement for male sexual enhancement. Read More »
Published May 6, 2011
The Council for Responsible Nutrition (CRN), Washington, D.C., recently submitted comments to FDA regarding the agency’s proposed rule for the health claim on phytosterols and risk of coronary heart disease. Douglas MacKay, ND, vice president,… Read More »

