Who Should Listen: Trial sponsors, clinicians, medical device developers, and site personnel looking to monitor complex processes with minimal error, fewer resources, and lower costs.
What You'll Learn: Join our panel of experts for this roundtable discussion to learn more about how the use of a technology-amplified, real-time, risk-based "just-in-time," approach to monitoring can help you:
- Ensure integrity of trial data and patient safety
- Optimize trial efficiency and quality
- Streamline sponsor, CRO, and trial site team interaction
Presenters:
- Marie Hanley
Vice President, Global Quality Services, Clinipace Worldwide - Monika Frey
Vice President of Global Clinical Operations, Clinipace Worldwide - John C. Parnell, RPh, MHA
Director, Global Clinical Monitoring, Clinipace Worldwide - Deborah Rosenfelder
Clinical Trials Manager, Clinipace Worldwide
