Topics
- Pre-clinical pharmacology research
- Current pediatric regulations within the FDA and EMA
- Innovative specialized models for pediatrics and neonatal patients
- Adult data to be effective in pediatric patients
- Overcome delivery, pediatric drug formulation and palatability challenges
Who should Attend
Vice Presidents, Heads, Director responsible for: Pharmacology, Clinical Pharmacology, Modeling and Simulation, PKPD, Medical Affairs and Pharmacometrics.
