Date :
Place : United States, Cambridge
Contact Person:Paula Edwards
Description:
Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part of the regulators that demands, in turn, that industry be keenly aware of the legal and regulatory duties, as well as key recent trends in enforcement activities by the Federal Government. This course will explore in detail what FDA requires of drug and device firms as well as recent current hot buttons in FDA enforcement activity for the advertising arena.Deadline for abstracts/proposals : 6th November 2017
Organized By :New York Events List
Keynote Speakers : Michael A Swit, Esq. FDA Lawyer Michael A. Swit focuses on solving the legal challenges confronted by the pharmaceutical, medical device, and other life sciences industries in tackling the myriad of legal mandates enforced by the U.S. Food & Drug Administration. Mr. Swit has extensive experience counseling life sciences firms on the demands of compliance with FDA's statutory and regulatory
Conference Highlights :The basics of FDA law and regulations governing advertising and promotion, as well as sister agencies such as the Federal Trade Commission, which shares jurisdiction with FDA on certain regulated products (e.g., OTC drugs). The distinctions between labels, labeling and advertising and how that impacts FDA's powers, and How to properly position Direct-to-Consumer (DTC) promotions
Venue :Cambridge, MA 02139, United States
Check the event website for more details.