FDA Regulation and Legislation of Cosmetics
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Online Webinar by
Online Compliance Panel
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Details
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.
Objectives of the Presentation
Objectives of the Presentation
- 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
Outline
Why Should you Attend
The webinar will cover laws and regulations for successful marketing and compliance of cosmetics in the U.S. It will help clarify what claims and product labeling are appropriate for cosmetics to market them successfully and avoid problems with FDA compliance. Current FDA Warning letters will be discussed to understand FDA's changing views on cosmetic enforcement. Adverse Event Reporting for Cosmetics will be discussed with focus on how this will change under the Personal Care Products Safety Act.
Areas Covered
The webinar will cover laws and regulations for successful marketing and compliance of cosmetics in the U.S. It will help clarify what claims and product labeling are appropriate for cosmetics to market them successfully and avoid problems with FDA compliance. Current FDA Warning letters will be discussed to understand FDA's changing views on cosmetic enforcement. Adverse Event Reporting for Cosmetics will be discussed with focus on how this will change under the Personal Care Products Safety Act.
Areas Covered
- FDA regulations for Cosmetics in the USA
- FDA Cosmetic Labeling requirements
- Cosmetic claims issues
- How can "Cosmeceuticals" be legally marketed?
- Proposed Cosmetics legislation: The Personal Care Products Safety Act
- How Adverse Event reporting requirements are changing for U.S. Cosmetics
Speaker/s
Instructor Profile:
Norma Skolnik works as a regulatory consultant to FDA regulated companies and to firms who wish to launch products in the U.S.A. Norma has over 35 years of U.S. regulatory experience, starting in the pharmaceutical industry. She was the Associate Director of Regulatory Affairs at Lederle Laboratories in Pearl River, N.Y. and then became Associate Director of Regulatory Affairs at Lederle Consumer Health where she helped launch Centrum and Caltrate dietary supplements. When Lederle was acquired by Wyeth, she became Associate Director of Regulatory Affairs there, acquiring more experience in the Dietary Supplement and OTC drug fields. She joined Warner-Lambert Consumer Health division in 1998 and became Assistant Director of Adams Regulatory Affairs. In 2002, when Pfizer acquired Warner Lambert she was promoted to Director of Regulatory Affairs for the Adams division. Adams was acquired by Cadbury-Schweppes in 2003 and she served as Cadbury Adams' Director of Regulatory Affairs for the Americas from 2003 until her retirement in 2008.
Norma earned a Bachelor's degree in Biology from the University of Cincinnati and holds a Master's degree from Pratt Institute in Brooklyn, New York. She's also done graduate work at Columbia University and Montclair State University.
Norma Skolnik works as a regulatory consultant to FDA regulated companies and to firms who wish to launch products in the U.S.A. Norma has over 35 years of U.S. regulatory experience, starting in the pharmaceutical industry. She was the Associate Director of Regulatory Affairs at Lederle Laboratories in Pearl River, N.Y. and then became Associate Director of Regulatory Affairs at Lederle Consumer Health where she helped launch Centrum and Caltrate dietary supplements. When Lederle was acquired by Wyeth, she became Associate Director of Regulatory Affairs there, acquiring more experience in the Dietary Supplement and OTC drug fields. She joined Warner-Lambert Consumer Health division in 1998 and became Assistant Director of Adams Regulatory Affairs. In 2002, when Pfizer acquired Warner Lambert she was promoted to Director of Regulatory Affairs for the Adams division. Adams was acquired by Cadbury-Schweppes in 2003 and she served as Cadbury Adams' Director of Regulatory Affairs for the Americas from 2003 until her retirement in 2008.
Norma earned a Bachelor's degree in Biology from the University of Cincinnati and holds a Master's degree from Pratt Institute in Brooklyn, New York. She's also done graduate work at Columbia University and Montclair State University.
Special Offer
Webinar Link: https://goo.gl/xS94QF
Special Offers :
- Use Coupon code " TNOI9Y " to avail a 10% discount on Recorded Session, Training CD or Flash Drive.
- Register For This Webinar & Get 40% Off On Next Upcoming Webinar Purchase - Use ORDER ID as PROMO CODE
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Onlinecompliancepanel is a dedicated team of youngsters, who work in tandem with the latest US FDA regulations/regulatory compliance in creating training sessions suitable for individuals and corporations. These sessions are simple, interactive and cost effective. We are a predominantly web based information exchange forum. Our interactive training sessions could be beneficial to corporations thriving in industries such as pharmaceuticals, drugs and chemicals, FDA compliance, medical devices, packaging and labeling, food and beverages, banking and finance, audits and inspections, recalls and crisis management and many more. We emphasizes in offering regulatory compliance training to compliance professionals on varied topics. These primarily include risk management, quality management, corporate compliance and other regulatory compliances. Some of our primary areas of focus include advancement and updates in regulatory compliance, best practices, risk management and market trends.
Professional training, in the essential quality disciplines, contributes to both the competitiveness of your business and also to personal motivation; it broadens the experience and accelerates the development of those who participate. We provide training in a number of ways: ...
Professional training, in the essential quality disciplines, contributes to both the competitiveness of your business and also to personal motivation; it broadens the experience and accelerates the development of those who participate. We provide training in a number of ways: ...
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