Overview of otc drug labelling requirements

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WEDNESDAY APRIL-30-2014

01:00 PM | 02:00 PM – EST DURATION: 60 MINUTES

Live webinar on "Overview of OTC Drug Labelling Requirements" DESCRIPTION The webinar will cover how OTC drugs can be effectively marketed in the U.S. and the OTC monographs and their importance to compliance in general and drug labeling in particular. FDA Drug Facts Labeling regulations and related requirements will be covered in depth. Why should you attend : In order to market OTC drugs in the U.S. it is essential to understand FDA regulations, labeling requirements and trends in FDA regulation. Understanding the OTC monograph system will help assure compliance and enable those who want to market products in the U.S. to make optimal use of FDA monographs to achieve the best OTC product claims and labeling. Areas Covered in the Session: 1. How OTC drugs can be marketed in the U.S. 2. OTC Monographs and their importance to compliance and Drug Labeling. 3. FDA Drug Facts Labeling Regulations. 4. How to achieve the best claims for your OTC product. Who will benefit: (Titles) Regulatory Affairs Associates, Specialists, Managers & Directors; Sales & Marketing Managers; Compliance Specialists & Officers. Anyone looking to market, label and promote OTC drugs in the U.S. will benefit from this presentation. Webinar Includes: Q/A Session with the Expert to ask your question PDF print only copy of PowerPoint slides 60 Minutes Live Presentation Certificate of Attendance


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Overview of otc drug labelling requirements by kevin c2go - Issuu