FDA Regulations and New Legislation for Marketing Cosmetics in the U.S

The webinar training will cover FDA regulations for marketing cosmetics and help attendees learn about new proposed legislation which will place new requirements on cosmetic product marketing in the U.S.

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One User Unlimited access to all recorded webinars for 6 Months

Recorded Version Only

(PPT + Recorded Streaming Link)

1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section
Last Recorded Date: Apr-2019

Download File Only

(PPT + Recorded Training File)

Downloadable file is for usage in one location only.
(For multiple locations contact Customer Care)
Downloadable link along with the materials will be emailed within 2 business days
Customer Care

Fax: +1-650-362-2367

Email: customercare@fdatrainingalert.com

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Learning Objectives:

By attending this webinar, participants will be able to:

  • To learn FDA Labeling requirements for Cosmetics & Personal Care Products
  • To understand cosmetic claims and compliance issues and how to avoid FDA issues
  • Learn what “Cosmeceuticals” are and how they can be legally marketed
  • Learn about 2015 Proposed Cosmetics legislation, the Personal Care Products Safety Act
  • Gain understanding of Good Manufacturing Practice systems for Cosmetics & Coming GMP regulations
  • Learn Adverse Event Labeling & Reporting requirements for cosmetics and how these will change under the Personal Care Products Safety Act
Areas Covered in the Webinar:
  • Laws and Regulations Applicable to U.S. Cosmetics
  • Cosmetic Labeling Requirements
  • Adverse Event Reporting for Cosmetics
  • Cosmetic Claims and Compliance Issues
  • Current Cosmetic GMP Requirements
  • 2015 Proposed Cosmetics Legislation: The Personal Care Products Safety Act
Who Will Benefit:
  • Regulatory Affairs Managers and Associates
  • QA Managers
  • Cosmetic Marketing Managers
  • Attorneys
  • Anyone interested in learning about cosmetic regulations and new proposed legislation
Instructor Profile:
Norma Skolnik Norma Skolnik

Regulatory Consultant, EAS Consulting Group and NS Consulting

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 as associate director of marketed product support for Lederle Laboratories and associate director of regulatory affairs for Wyeth. She currently works as a regulatory consultant.

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@fdatrainingalert.com call +1-888-771-6965 (Toll Free).

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