In order to market dietary supplements successfully in the USA and to avoid regulatory problems, it’s essential to understand US FDA dietary supplement regulations.
This webinar with expert speaker Norma Skolnik will cover essential and significant regulations for the marketing and labeling of US dietary supplements. It will also cover permissible dietary supplement claims and ways to avoid regulatory challenges that could get a company in trouble. References to all FDA regulations and policies regarding Dietary Supplements will be provided as well as know-how tips for marketing dietary supplements without regulatory issues.
Who should attend?
Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.
- Larry D. Bowe , BS, CFPMT, CFPMP
- Natasha Rowley-Phipps,
- Joe Lynch and John Condon,
- Dr. John M. Ryan, Ph.D.
- Dr. Keith Warriner and Dr. Azadeh Namvar,
- Norma Skolnik,
Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that, she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and...
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