Preview: Next Level Medical Affairs Leaders Forum 2014

Preview: Next Level Medical Affairs Leaders Forum 2014

The convergence of payer and regulator evidence requirements warrants a strategic evidence generation plan and a mindful orchestration of peri and postapproval real-world studies.  Study designs resulting in a diverse array of health economic and safety data are increasingly warranted to meet the demands of various stakeholders. 

Next week, Medical Affairs, Regulatory professionals, and industry experts will gather in Berlin, Germany, to discuss designing and implementing observational and registry studies to achieve medical, pharmacovigilance, and market-access objectives.  UBC’s Krista Payne, MEd, Executive Director, Value Demonstration, and Dr. Janine Collins, Senior Director, European Safety and Risk Management, will present “Navigating the Convergence of Payer and Regulator Evidence Requirements; Opportunities and Challenges”.

Join the session Wednesday, February 12, as our speakers discuss:
• Landscape trends in peri and postapproval observational research
• Strategic evidence generation
• Cost and time-efficient “hybrid” study designs
• Integration of HEOR outcomes in Post-authorization Safety Studies (PASS)
• Optimizing cost and timeline efficiency through strategic evidence generation over the late-phase product lifecycle

We look forward to connecting with you!