Beyond Pharmaceuticals: Research Involving Cosmetics, Conventional Foods, and Dietary Supplements
It can sometimes be tricky to determine the regulatory framework applicable to research involving cosmetics, conventional foods, and dietary supplements. With just a few specific changes, a simple study with limited regulatory requirements can morph into a trial requiring much more oversight.
How do you know which regulations apply to your particular study?
In this webinar, Advarra regulatory and human subject protections experts Constance Cullity, Senior Director of Regulatory Compliance, and Susan Ebert, Senior IRB Chair Director, discuss the various regulatory frameworks potentially applicable to these unique research fields. They also describe how to identify when foods, dietary supplements, or cosmetics are being studied as a drug – and the requirements accompanying that distinction.
Learning Objectives:
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Define key terms informing the appropriate regulatory framework for research involving cosmetics, conventional foods, and dietary supplements
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Recognize the regulatory frameworks potentially applicable to research involving cosmetics, conventional foods, and dietary supplements
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Identify when a cosmetic, conventional food, or dietary supplement is being studied as a drug
Presented By

Constance Cullity
MD, MPH, CIP
Senior Director, Regulatory Compliance
Advarra

Susan Ebert
MS, RD, CIP
Senior IRB Chair Director
Advarra
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DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour