Pharmaceuticals and biotech companies routinely undergo medical, legal, and regulatory (MLR) review to ensure that their products’ claims, promotions, and training programs are medically accurate and compliant with FDA standards and other regulations.
- The current regulatory landscape
- How the lack of warning letters raises the challenges to staying compliant with the review materials
- Social media platforms’ compliant execution
- Co-promotion of drugs
- Artificial intelligence tools that simplify the review processes
- …and more!
2023 TESTIMONIALS
2023 Speaking
Faculty
Christi Bruce
SANOFI
Bradley Carlson
MALLINCKRODT PHARMACEUTICALS
Brooke Deans
MALLINCKRODT PHARMACEUTICALS
Zoe Dunn
HALE ADVISORS
Georgia Gayle
ALEXION PHARMACEUTICALS
Larry Herring
MERZ AESTHETICS
John Paul Marcus
TRAVERE THERAPEUTICS
Heather McFalls
ORGANON
Lav Patel
MERCK
Kavita Rana
INSMED INCORPORATED
Melissa Sadowski
OTSUKA
Kristi Sanford
UCB
Marianne Slivkova
STEMLINE THERAPEUTICS
Gary Wieczorek
ABBVIE
Alexander Zachos
TAKEDA
2024 SPONSORSHIP OPPORTUNITIES ARE OPEN
Sponsorship is a great way to enhance your brand’s visibility and help you connect with top-level decision-makers, innovators, and industry disruptors. There are a number of ways to maximize branding opportunities at the summit.
TOP REASONS TO ATTEND
WHO SHOULD ATTEND
This event is designed for pharmaceutical, biotech, and medical device professionals with responsibilities in the following areas:
All the key players that perform Promotional and Legal Regulatory Reviews:
- Promotional Review / Promotional Materials / PRC / MPRC / PMRC
- Regulatory Promotion & Advertising / AdPromo / AdProm / PromoAd
- Compliance
- Regulatory Affairs
- Marketing Operations
- Medical Affairs
- General Counsel & Legal Affairs
- Medical Information/Writer
- Advertising & Promotion
- Content & Social Media Marketing
- Medical Communications/MSL
- Copy Editors
- Labeling
- Medical Affairs
- Commercial Operations
- Health Economics / Outcomes / HEOR