You will be redirected to our secure system.
When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.
Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.
In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.
Learn moreRemember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.
“Since in many countries, Personal Care products do not require Health Authority review and approval prior to marketing, there is often confusion about what product claims can be made, what labeling is required, and what ingredients cannot be used. Without knowledge of the regulations in each country, non-compliant product is often detected by Health Authorities once the product enters the marketplace. This typically results in a costly product recall.
This intensive 12-hour accredited ON DEMAND course will provide an in-depth overview of the regulatory requirements for personal care products in the United States and the European Union, including additional requirements in the states.
It will review the regulatory bodies, enforcement tools and the relevant legislation and guidance to inform regulatory compliance. This will include key agencies having jurisdiction over cosmetics, with emphasis on the U.S. FDA, the European Commission, and the state of California, among others.
There will be a detailed discussion of ingredient restrictions based on their function in the finished formulation. In addition to a full review of labeling requirements, we will consider how claims impact a product’s regulatory classification and its acceptability to the regulator, with examples to demonstrate the restrictions, risks and current enforcement priorities.”
This course is intended for all those involved in the regulatory aspects of cosmetics, OTC drugs and personal care products especially:
– Regulatory Affairs Practitioners, including Attorneys and Paralegals
– Corporate compliance officers
– Marketing Personnel
– Research and Product Development Personnel
– QC and QA Professionals
Jennifer R. Martin
Director of Regulatory Affairs North America and Global Skin Health for the Colgate-Palmolive Company
Jennifer R. Martin is Director of Regulatory Affairs North America and Global Skin Health for the Colgate-Palmolive Company and a longtime regulatory affairs and product safety professional. She has more than 30 years of experience in analyzing legislation and regulation and applying it to assure product safety and compliance for cosmetics, drugs, medical devices, foods, pesticides, household cleaning products and consumer goods, including children's products and art materials.
Some of her achievements include:
Built the FDA compliance function for a $10BB retailer with more than 3,000 stores selling thousands of SKUs
Established a global Medical Affairs oversight function responsible for worldwide monitoring of consumer post-market experience
Created corporate consumer products compliance programs with commensurate pillars of policy, process and governance
Jennifer has a Master's degree in International Affairs from the American University School of International Service and a Certificate in Consumer Product Safety from the John Cook School of Business at St. Louis University.