Overview

Tutorials are not included in the meeting registration and require a separate registration fee.

If you are new, or relatively new, to the preparation or review of advertising and/or promotional materials, this tutorial is for you!! This tutorial is designed to provide background information to attendees of the DIA program to enable better understanding of the conference content. The leaders will provide an introductory foundation for anyone working in our current regulatory environment. Whether you are a regulatory, legal, medical, compliance, or marketing professional, the information will be interesting, practical, and vital!

Lunch will not be served for a half day tutorial.

Who should attend?

This tutorial is designed for individuals within the pharmaceutical and biologics industries that are
involved in:

marketing
legal
regulatory
compliance
communications

If you are relatively new to this area, please join our experienced experts to gain the important information you need to maximize your workshop learning!

Learning objectives

At the conclusion of this tutorial, participants should be able to:

Discuss the current regulatory/compliance environment pertaining to prescription drugs, biologics and medical devices as relevant to the DIA program content.
Describe the FDA advertising and promotional requirements, including such topics as (as relevant to the final program content): claim support requirements, fair balance expectations, internet and social media challenges, product booths at medical conventions, adherence and preference programs, patient involvement and outreach, disease state programs, and public relations challenges

Have an account?

Tutorial: OPDP/APLB 101: A Primer Based on Today’s Changing Environment

Overview

Who should attend?

Learning objectives

Be informed and stay engaged.