Online Training 2015 - FDA Regulations for Marketing OTC Drugs in the U.S. - By Compliance Global Inc

Overview:
The webinar will offer an overview of FDA requirements for marketing, labelling and promotion of OTC drugs in the U.S. It will cover how OTC pharmacy can be effectively marketed and the OTC Monographs and their importance to compliance in general and drug labels in particular. Challenges of marketing OTC drugs in the U.S. will be covered.
Why Should You Attend:
Attendance is important to assure that your OTC drug products are in compliance with FDA food regulations and to learn about how the OTC monographs can help you market your drug products effectively. Helpful references to websites and relevant regulations and know-how tips will also be provided.
Areas Covered in the Session:
? Background and History of OTC Drug regulations
? Different Ways that OTC Drugs can be Marketed in the U.S. (NDA, Rx to OTC Switch vs. Monograph process)
? Overview of the OTC Drug Monographs and Their Importance
? FDA Drug Facts Labelling Requirements
? FDA Regulations for Required Adverse Event Reporting
Learning Objectives:
? To become familiar with FDA regulations for marketing OTC drugs in the U.S.
? In-turn assure compliance and more effectively market OTC products
Who Will Benefit:
? Regulatory Affairs Managers and Associates
? QA Managers
? OTC Drug Marketing Managers
? Anyone interested in learning about U. S. OTC Drug regulatory requirements and compliance
Level:
Intermediate
For more detail please click on this below link:
https://www.complianceglobal.us/product/700172
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515