May 13–15, 2020

7th Promotional Review Committee Compliance & Best Practices — Midwest

Royal Sonesta Chicago Riverfront

Chicago, IL

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Past Attendees

Click here to view previous attendees of the midwest series
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Sponsorship Inquiry

Share expertise, showcase your technologies, products & service
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Reserve Your Seat

Register now to get Early Bird Pricing
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WHAT TO EXPECT

Join the leading industry event for improving PRC teamwork and speed while maintaining expertise even with changes in team composition and regulatory expectations. No other event offers such in-depth technical and operational strategy from such a large faculty of your peers!

Attend to gain new strategies for:
  • Complexity-based tiering of PRC responsibilities
  • Maintaining team skills and readiness during mergers, acquisitions, and divestitures
  • Managing document access and accuracy despite of regular turnover
  • Efficiently leading PRCs amidst high material volume
  • Developing CAPAs to gauge committee performance
  • Complying to the FDA’s latest rule on Combination Product safety (PMSR) requirements
  • EU regulations vs. US regulations
  • Multi-channel social media trends

                              MEET THE CHAIRPERSON 

Linda Pollitz, 

Senior Director, Regulatory Affairs, Advertising & Promotional Labeling, 

ALKERMES

Learn More about Speaker Group

CONFIRMED SPEAKERS INCLUDE

Sabrina Mays-Diagne, 

Senior Corporate Attorney, 

OTSUKA PHARMACEUTICALS 

Madhavi Bellam 

Director, Regulatory Affairs, Global Advertising and Promotion 

ABBOTT

Janet Gottlieb, Ph.D., 

Executive Director, Global Medical Promotional Review

ALLERGAN

Alana Goodman  

Director, Global Marketing Operations 

ALEXION PHARMACEUTICALS 

Khaudeja Bano 

Senior Medical Director, Head of Medical Affairs 

ABBOTT MOLECULAR

Top Reasons to Attend

  • Optimize leadership, teamwork, operational skills and speed of promotional review committees through learning at targeted workshops and sessions
  • Internal Stakeholder panel featuring marketing, legal, and operational committee members from a leading organization’s PRC
  • Sessions regarding specific promotional strategies and review committee considerations
  • Workshops and in-depth sessions focusing on OPDP expectations and DOJ enforcement trends
  • Network with the industry’s leading and most experienced regulatory experts

WHO ATTENDS

This conference is designed for professionals from pharmaceutical, biotechnology and medical device companies, advertising agencies, CRM/ Data Management software suppliers, law firms, and regulatory consultants. Attendees' job responsibilities include:

  • Promotion Review/ Promotional Review / PRC
  • Material/ Clinical Review
  • Regulatory Promotion and Advertising
  • Regulatory Affairs/ Regulatory Process/ Compliance
  • Labeling
  • Medical Affairs/ Medical Review
  • Program Review/ Review Operations / Program Review Operations

 

This event is also of interest to

  • CRM / Data Management Software Suppliers

  • MLR Process Vendors and Facilitators
  • Advertising /Marketing Agencies
  • Regulatory Consultants
  • Medical Writing Firms
  • Law Firms
  • Editor/ Editorial Review / Copy Editing
  • Medical Information
  • Medical Communications / Medical Information/ Medical Science Liaison / Director
  • Marketing / Marketing Operations / Marketing Communications / Marketing Services
  • Commercial Operations
  • Brand Manager / Product Manager / Brand Marketing
  • Legal Affairs / Counsel / Regulatory Counsel