Meeting FDA requirements for OTC Drug Labeling - Webinar by GlobalCompliancePanel

Date	Dec 4, 2013
Time	01:00 PM EDT
Cost	$225.00
Online

Overview: The webinar will help participants review and understand FDA requirements for OTC Drug labeling and compliance. OTC Monographs and their importance to OTC Drug marketing in the U.S. will also be covered. 

Why Should You Attend: Anyone who wants to market OTC drugs in the U.S.A. and assure that they're labeled properly with appropriate claims will benefit from this program/webinar. It will provide background for OTC Drug labeling regulations and an understanding of how to comply with FDA requirements. Potential FDA enforcement actions regarding OTC drug labeling will also be covered.

Areas Covered in the Session:

• OTC Drug Labeling regulations: background and requirements
• Drug Facts labeling
• OTC Monographs and their importance
• Conditions under which OTC Drugs can be marketed in the U.S.A.

Who Will Benefit: Anyone who wants to market OTC drugs in the U.S.A. and assure that they're labeled properly with appropriate claims will benefit from this program/webinar: 

• Regulatory Professionals
• Drug Marketers
• Manufacturers and Distributors
• Students of FDA Regulations

Norma Skolnik has 30 years of regulatory experience in the OTC Drug, Food and Dietary Supplement industries. She has had extensive experience advising on regulatory strategies for new and marketed consumer healthcare products. Particularly regarding the development and review of optimal product claims and advertising. For 10 years, Norma served as Director of Regulatory Affairs for Cadbury Adams, Americas (formerly Adams Division of Pfizer).

NetZealous LLC,
DBA GlobalCompliancePanel 
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA          
USA Phone:800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com    
http://www.globalcompliancepanel.com

Event Link - http://bit.ly/1aFPxve