Back to Pharmaceuticals: Advertising and Promotional Labeling in the US
4.00 RAC

Pharmaceuticals: Advertising and Promotional Labeling in the US

This course outlines the regulatory framework for prescription drug and biologic promotional materials by examining FDA regulations and issues involved in producing compliant promotional materials. Practical aspects for the review of promotional materials will be provided, along with key evidentiary standards required to substantiate claims. Emerging trends in promotion (i.e., use of social media) will also be discussed.


Credits:
4.00 RAC

  • List Price: $495.00
  • Member Price: $360.00

 
Want to save more?
to see if you qualify for a lower rate.
Members: save $135.00 or more
Item Details:

This course outlines the regulatory framework for prescription drug and biologic promotional materials by examining FDA regulations and issues involved in producing compliant promotional materials. Practical aspects for the review of promotional materials will be provided, along with key...

Back to Pharmaceuticals: Advertising and Promotional Labeling in the US
View More

» View the Table of Contents

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