Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements

PALO ALTO, Calif. - May 24, 2013 - PRLog -- Why Should You Attend:

In the last 4 years the number of FDA warning letters to manufactures of dietary supplement manufacturers have seen a significant increase. FDA now requires manufacturers of dietary supplements to follow GMP requirements closer to those for drugs than those for foods. These requirements include stricter documentation, standardized processes, use of trained personnel, adequately designed facilities, quality testing, packaging and shipping, and audit trails of processes. These requirements have created lots of anxiety in an industry filled with small businesses with few products, and international companies marketing in the US.

If you are a manufacturer, importer, supplier, stocker, marketer, shipper, or user of dietary supplements, this training is for you. The webinar will describe the US GMP requirements and discuss techniques to be compliant using easier, shorter and convenient strategies. The presenter will discuss ways to demonstrate compliance to the current regulations and regulatory trends for the near future. Common findings and possible solutions will be discussed. Case studies will be presented for audit experiences in many countries including US, China, Israel, Taiwan, and India.

For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701922?channel=PRlog