On-Demand Content | Virtual Event

The need to review and update your pharmaceutical labeling practices has never been greater with the recent FDA definition of “intended use” and the final verdict in “GSK vs Teva.”

The FDA Pharmaceutical Labeling Boot Camp offers a uniquely deep dive not only into labeling best practices, but in how to align your labeling standards with your overarching marketing compliance strategy.

Via our fully interactive platform, don’t miss your chance to network with colleagues, as well hear from industry leaders as they provide tips and best practices you can put into practice immediately.

SPEAKER HIGHLIGHTS

Shital Bhammar
Shital Bhammar
Senior Manager, Labeling Design, Global Patient Supply

BLUEBIRD BIO

Christi Bruce
Christi Bruce
Head of Promotional Excellence and Standards for Advertising and Promotion

SANOFI

Howard Dorfman
Howard Dorfman
Adjunct Professor

SETON HALL UNIVERSITY

David Hampton
David Hampton
Director, Global Regulatory Labeling Operations

TAKEDA

Kate Kocik
Kate Kocik
Director of Labeling Compliance

TAKEDA

Megann Looker
Megann Looker
Executive Director, Head of Global Labelling

JAZZ PHARMACEUTICALS

Roger Peterson
Roger Peterson
Manager, Global Labeling Systems

ARTHREX

Lee Rosebush
Lee Rosebush
Partner

BAKER & HOSTETLER LLP

Matthew Sample
Matthew Sample
VP, Manufacturer Operations

AMERISOURCEBERGEN

Marc J. Scheineson
Marc J. Scheineson
Partner

ALSTON & BIRD LLP

Josephine Secnik
Josephine Secnik
Director of Regulatory Affairs

ELI LILLY

Remon Zakhary
Remon Zakhary
Associate Director, Packaging Design & Development

BAYER

TOP REASONS TO PURCHASE

  1. Discuss methods of developing social media campaigns that remain compliant with current regulations
  2. Interact with your peers to discuss changes to “skinny-labeling” post ‘GSK v Teva”
  3. Take part in detailed conversations on the FDA’s definition of “Intended Use”
  4. Work with your peers to assess labeling requirements associated with combination products
  5. Network with industry executives and gain tips and best practices that can be put into effect immediately.

WHO SHOULD PURCHASE

This event is designed for pharmaceutical, biotech, and medical device professionals with responsibilities in the following areas:

  • Regulatory Affairs
  • Legal Affairs/Compliance
  • Promotional Review
  • Brand Marketing and Labeling
  • Medical Affairs
  • Medical Information
  • Corporate Communications
  • Commercial Operations
  • Medical Education
  • Medical Communication
  • Healthcare Compliance and Privacy
  • Brand Management
  • Sales
  • Product Training
  • Quality Assurance

Secondary Market:

  • Regulatory Affairs Consultants
  • Law Firms
  • Promotional Review Vendors
  • Compliance Service Providers
  • Marketing/Advertising Agencies
  • Data Management Software Vendors
  • MLR Process Vendors and Facilitators

MEDIA PARTNERS