Leveraging MIDD to Shape Development Strategy & Evidence Generation

9:30 am - Thursday 19th November 2026

  • Moving beyond the use of MIDD solely for regulatory submissions to support critical development and lifecycle management decisions
  • Using quantitative evidence to inform dosing, special populations, benefit-risk assessments, and broader clinical development strategies
  • Case studies demonstrating how MIDD has influenced regulatory discussions, development plans, and cross-functional decision-making

Speakers:

Associate Director
Bristol Myers Squibb