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By Todd Harrison & Paul Feinstein
Published January 2, 2012
Revisions to the notification guidance must be more reasonable and less restrictive. 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 »
By Douglas Kalman
Published June 1, 2010
Stick with the regulatory definition of substantiation and you will be ahead of the curve. Read More »
By Todd Harrison
Published June 1, 2010
We have entered a new regulatory era, so make sure your products are safe and the claims are substantiated. Read More »
By Paula Brown and Dr. Katherine Sharpless
Published June 1, 2010
NIST specialist reviews certified reference materials. Read More »
By Erik Goldman
Published May 3, 2010
Experts agree increased regulation is on the horizon, but to what degree can and should be determined by industry.
Read More »
By Paula Brown & Dr. Joseph Betz
Published April 1, 2010
A tale of chemical calibration standards. Read More »
By Douglas Kalman
Published April 1, 2010
Industry must be more proactive in FDA’s decision-making processes. Read More »
By Todd Harrison
Published January 6, 2010
FDA guidance suggests the agency may be devoting more attention and enforcement resources to preventing liquid dietary supplements from being marketed as beverages. Read More »
By Douglas Kalman, PhD
Published June 1, 2009
Companies are best served by conducting their own product-specific or ingredient-specific research in today's market. Read More »
By Todd Harrison
Published June 1, 2009
Monitoring the safety of products has never been more important for dietary supplement manufacturers. Read More »
By Jeff Crowther
Published May 1, 2009
Exploring adulteration in China and how to avoid it. Read More »
By Paula Brown
Published April 1, 2009
Ensuring product integrity may be the industry's biggest challenge yet. Read More »
By Todd Harrison & Jennifer Thomas
Published April 1, 2009
FDA's decision regarding pyridoxamine has larger implications for dietary ingredients in general. Read More »
By Douglas Kalman, PhD
Published January 1, 2009
If FDA gets its way, probiotics and other health ingredients could be reclassified as drugs in the future. Read More »
