First round of Abstract Submissions is open now..!
Don't miss the opportunity! Submit your abstract for the first round by November 28, 2025.

 

Regulatory Science & Drug Approval Strategies

The changing regulatory environment, scientific frameworks, and tactical methods required to successfully negotiate drug approval procedures globally are the main topics of this session. Participants will examine international regulatory frameworks, data needs, and risk-benefit analysis that are critical to effectively and safely delivering novel treatments to patients.

  • Regulatory Strategy
  • FDA/EMA/PMDA Guidelines
  •  Risk–Benefit Assessment
  • Safety Data Integration
  • Lifecycle Management.
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