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May 2012
Last Updated Saturday, May 26 2012
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Search Results for 'FDA'

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Published March 1, 2011
The dietary supplement industry’s leading trade associations have joined forces with FDA to support heightened efforts aimed at addressing significant public health problems posed by products that are illegally marketed as dietary supplements b… Read More »
Published February 4, 2011
Daniel Fabricant, PhD, announced his resignation as vice president of global government and scientific affairs with the Natural Products Association, Washington, D.C. He will be joining FDA as director, Division of Dietary Supplement Programs at the… Read More »
Published January 13, 2011
Earlier this week, the Council for Responsible Nutrition (CRN), Washington, D.C., submitted comments to FDA regarding Investigational New Drug (IND) applications, with an emphasis on providing further clarification on dietary supplements and food components and drugs, as well as acknowledging the inherent differences between all of these products. Read More »
Published December 15, 2010
The dietary supplement industry’s leading trade associations today joined forces with FDA to support heightened efforts to address significant public health problems posed by products that are illegally marketed as dietary supplements but contain the same active ingredients as FDA-approved drugs or other ingredients that do not qualify as dietary ingredients. Read More »
Published November 9, 2010
BioScreen Testing Services, Los Angeles, CA, recently hosted a delegation of 25 officials from the Chinese Food and Drug Administration of Chongqing City P.R. China. Over a three-week period, the officials travelled throughout the U.S. to gain a bett… Read More »
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Published October 11, 2010
FDA has warned that Slimming Beauty Bitter Orange Slimming capsules contain the active pharmaceutical ingredient sibutramine, a prescription-only drug that is a stimulant. Read More »
Published July 2, 2010
Members and staff for the Global Organization for EPA and DHA Omega 3s (GOED) met with FDA officials this week to discuss regulations and DRIs for omega 3s. Read More »
Published June 21, 2010
FDA has warned consumers that Magic Power Coffee, an instant coffee product marketed as a dietary supplement for sexual enhancement, contains an active drug ingredient that can dangerously lower blood pressure. Read More »
Published June 9, 2010
Greens powders—made from wheat grass, alfalfa, kelp, spirulina, leafy vegetables and other chlorophyll-containing ingredients—were recently tested by ConsumerLab.com, White Plains, NY, for potential contamination with heavy metals and pesticides. Read More »
Energy Ingredients for Baby Boomers
By Joanna Cosgrove
Published June 7, 2010
Opportunities abound in this very specific niche market. Read More »
An Interview with Michael Chernyak
By Sheldon Baker
Published June 4, 2010
Michael Chernyak is the founder of CK Nutritional Ingredients (CKNI), a Toronto, Canada-based marketer of innovative science-based raw materials to the natural health products industry. Read More »
GMP Deadline: Recess is Over
By Sean Moloughney
Published June 1, 2010
The month of June often conjures a variety of pleasant connotations, including the end of a school year and warmer weather, depending on your geographical location. Here on the east coast, we’ve emerged from a stormy winter and settled into a m… Read More »
The Research Process: Substantiation, According to FTC
By Douglas Kalman
Published June 1, 2010
Stick with the regulatory definition of substantiation and you will be ahead of the curve. Read More »
Bioenergy: Getting to the ‘Heart’ 
of the Nutraceuticals Market
By Rebecca Wright
Published June 1, 2010
Bioenergy, Inc., is an integrated biotechnology company based in Minneapolis, MN, which was founded by a pediatric cardiac surgeon, Dr. John Foker, who spent many years studying D-ribose’s effect on improving heart function. This pursuit led hi… Read More »
Published June 1, 2010
FDA should apply the same rigor to evaluating the science behind health claims of foods and dietary supplements as it devotes to assessing medication and medical technology approvals, a new report from the Institute of Medicine (IOM) stated. The comm… Read More »
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