On-Demand Webinar

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:

  • Define key terms informing the appropriate regulatory framework for research involving cosmetics, conventional foods, and dietary supplements
  • Recognize the regulatory frameworks potentially applicable to research involving cosmetics, conventional foods, and dietary supplements
  • Identify when a cosmetic, conventional food, or dietary supplement is being studied as a drug

Presented By

Connie Cullity.png

Constance Cullity

MD, MPH, CIP

Senior Director, Regulatory Compliance
Advarra

Susan Ebert.png

Susan Ebert

MS, RD, CIP

Senior IRB Chair Director
Advarra

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Who should watch?

Research professionals involved in planning, conducting, and overseeing research involving cosmetics, conventional foods, and/or dietary supplements, including: investigators, site staff, sponsor representatives, CRO representatives, and IRB members and administrators.

CE Credits

This session meets the Certified IRB Professional (CIP) recertification guidelines for a maximum of 1 credit.

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.

This event may qualify for continuing education (CE) credits. Please check with your professional organization(s) to determine whether the event meets their CE eligibility requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour

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