Back to On-demand Program: Advertising, Promotion and Labeling: the US Regulated Environment (2016)
5.00 RAC

On-demand Program: Advertising, Promotion and Labeling: the US Regulated Environment (2016)

An on-demand recording of the RAPS Virtual Program, Advertising, Promotion and Labeling: the US Regulated Market, originally recorded on 30 March 2016.


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5.00 RAC

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Hear leaders from industry, regulatory agencies and the legal profession share their expertise through presentations, discussions and case studies. This program examines current guidelines and expectations for healthcare product advertising, promotion and labeling in the US and how they impact the...

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Fundamentals of US Regulatory Affairs, Eighth Edition

Table of Contents

Section I: General Information
Chapter 1 FDA and Related Regulatory Agencies
Chapter 2 History of Food, Drug and Cosmetic Law
Chapter 3 Overview of Drug, Biologic and Device Regulatory Pathways
Chapter 4 FDA Communications and Meetings
Chapter 5 Preparing for Key FDA Meetings and Advisory Committee Meetings
Chapter 6 Crisis Management
Chapter 7 Health Technology Assessment
Chapter 8 Good Laboratory Practice Regulations
Chapter 9 Clinical Trials: GCPs, Regulations and Compliance
Chapter 10 Current Good Manufacturing Practice and Quality System Design