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

 

Preclinical Drug Development and Trial Design

This session delves into the essential period of preclinical research, in which promising drug candidates are examined for safety, effectiveness, and pharmacological qualities prior to entering human trials. Attendees will look at cutting-edge techniques, regulatory expectations, and novel study designs that improve the predictive potential of preclinical research and translational success.

  • In Vitro Models
  •  ADME Studies
  • Safety Pharmacology
  • First-in-Human Trials
  •  Animal Model Ethics
  •  Regulatory Requirements
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