ComplianceOnline

The Risk of Cosmetics and What it means to their Regulation

Instructor: Rob Ross Fichtner
Product ID: 704955
  • 18
  • January 2017
    Wednesday
  • 10:00 AM PST | 01:00 PM EST
    Duration: 90 Min

Live Online Training
January 18, Wednesday 10:00 AM PST | 01:00 PM EST
Duration: 90 Min

$199.00
One Dial-in One Attendee
$399.00
Group-Max. 10 Attendees/Location
(For multiple locations contact Customer Care)

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section 48 hrs after completion of Live training

Training CD

$299.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days after completion of Live training

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This webinar will discuss some of the major issues in the regulation of cosmetics. Upon completion of the session attendees will learn how regulators regulate cosmetics compared to other categories, fine line between cosmetics and drugs, and future directions for cosmetic regulations.

Why Should You Attend:

The regulation of cosmetics is often thought as “regulation light”, and a subject not taken seriously enough by those from outside of the category, or sometimes for those who are new to it. Anything could be further from the truth. Cosmetic regulations today are complex and becoming more so. Exacerbating the situation is that there is no harmonized global approach. Drugs and medical devices have by comparison far more consistent approaches, and receive a great deal of assistance from regulators in granting approvals. In many global markets, cosmetics simply arrive on store shelves and often the first intersection with a regulator is with a warning capable of threatening a company’s business.

This seminar will speak to some of the major issues in the regulation of cosmetics. While the focus will be on North America, there will be a general discussion on what regulatory framework this category deserves. What are the challenges facing both the industry and regulators? Where is the line between cosmetics and drugs? How do we deal with the exciting and challenging innovations such as cosmetic active ingredients, medical devices and nutritional supplements for beauty?

Learning Objectives:

From the seminar you will learn:

  • How regulators regulate cosmetics compared to other categories
  • The key issues regulating cosmetics
  • The very fine line between cosmetics and drugs
  • The roles of organizations influencing cosmetic regulations
  • Future directions for cosmetic regulations

Areas Covered in the Webinar:

  • Current approaches to the regulation of Cosmetics
  • Issues with Cosmetic Regulation
  • Organizations influencing regulations: governments, industry, NGOs
  • Future predictions for Cosmetic Regulation

Who Will Benefit:

  • Regulatory affairs
  • Research and Development
  • Marketing personnel
  • Manufacturers
  • Brand owners
  • Importers and Distributors
Instructor Profile:
Rob Ross Fichtner

Rob Ross Fichtner
President and CEO, Focal Point Research Inc

Rob Ross-Fichtner (President & CEO Focal Point Research Inc., Professor at Seneca College) has more than 35 years of experience in the formulation, manufacturing and regulation of cosmetics, drugs, medical devices and nutritional supplements. He has completed hundreds of regulatory submissions for product registration and approval, and has served as a consultant to companies of all sizes around the world pertaining to their Canadian and US compliance. He has also served as a consultant directly to Health Canada.

Rob has extensive experience inspecting Cosmetic and OTC drug facilities and developing QA programs in Canada, the US and in international locations. He also has many years of experience in Research and Development, including formulation, stability and analytical chemistry, clinical trials and manufacturing. He has served as an expert witness in litigation, and contributes regularly to the development of intellectual property.

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