The Cosmetic-Cosmeceutical Distinction: Walking the Line in Developing Label Claims - Webinar by GlobalCompliancePanel 2010
September 22, 2010(Ended)
Online Webinar
Drafting claims where you "walk the line" between cosmetic and drug
claims is an art with little existing practical guidance. Although
different experts can disagree about a particular claim, the labeling
regulations are based on a strong regulatory foundation. After a
discussion of pertinent U.S. laws and regulations, we extensively
examine actual claims and determine whether they cross the line We will
each examine claims to better understand the cosmetic/cosmeceutical
interface. It will be fast paced but fun! Then, you will have a chance
to ask questions about the presentation and related issues. By the end
of the presentation, you will be more able to develop cosmetic claims
with a lower regulatory risk.
Why you should attend: Cosmetic manufacturers are
driven by the need to have product claims that are at least as strong
as their competitors. At the same time, they are rightfully concerned
that if they cross the line and make a drug claim, they may be subject
to the misbranding provisions of the Act, which can lead to product
seizure, injunction and criminal action against companies or its
responsible people. You will learn who is watching over you when you
develop claims and how to reduce your regulatory risks.Areas Covered In the Seminar:
- How to distinguish between illegal and legal claims
- What makes a claim a cosmetic claim or a drug claim
- Which claims are lower risk than others and why.
- What is the meaning of Intended Use
- Misbranding
- False and Misleading
- The OTC Monograph
- The
role of the FDA, Federal Trade Commission (FTC) and other regulatory
and non-regulatory bodies can have in reviewing your claims
- Internet promotion
- Claims at trade shows
- What are the risks on non-compliance
- Warning Letters
- FTC Actions
- Minimizing problems in drafting claims.
Prices *
245 US Dollar (Early registration date: September 21, 2010)
Exhibition
No exhibition
Organization
Categories
Concurrent events
- Why Medical Device Companies Receive Warning Letters - Webinar by GlobalCompliancePanel 2010
- Preparing for FDA Inspections in a Changing Regulatory Environment - Webinar by GlobalCompliancePanel 2010
- Compiling the Design History File, and Technical File / Design Dossier - Webinar by GlobalCompliancePanel 2010
- The ICF Process: Tips on Achieving Optimal compliance and Comprehension
- Project Management Certification Study Group - Information Year 2010
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
