Join us for this webinar as we explore how natural history studies, including their use as external comparators and controls, can reinforce a robust regulatory strategy.
Key Topics:
- What kind of regulatory objectives can be achieved across the total product life cycle?
- Why are natural history studies critical for regulatory and evidence strategy?
- How can natural history studies help sponsors anticipate challenges and address gaps in their regulatory programs?
- What design considerations are critical for different study approaches?
Speakers:
Julien Heidt, MSc
Sr. Consultant,
Regulatory Science Strategy and Innovation, IQVIA
Tiffany Mercado, MSc
Associate Principal,
Regulatory Science Strategy and Innovation, IQVIA
Chinenye Ugoji, PhD, MPH, BPharm
Associate Director,
Global Epidemiology & Database Studies, IQVIA
