Nome da Sessão
Supercharge Your Site's Success: Billing Compliance for Investigational Device Trials
Data hora
quarta-feira, 22 de outubro de 2025, 11:30 - 12:30
Track
Billing Compliance
Descrição
Step into the world of investigational device trials and learn what it takes to stay compliant while advancing cutting-edge research. This session dives into the critical aspects of research billing compliance and documentation, giving you the tools to navigate regulatory requirements with confidence. From site operations to sponsor expectations, we will explore the must-know strategies for ensuring your device trial is both compliant and successful.
Learning Objectives:
- Distinguish billing requirements for investigational device trials.
- Explain documentation and reporting needs for device studies.
- Identify the unique coding requirements associated with approved device trials.
caixas de som
Polina Eshkol - Manager, Clinical Research Compliance - UCLA Health
Tanisha LaVeck - Clinical Research Financial Analyst - Holy Cross Health – Research Department
Geoffrey Schick - Director, Strategic Site Partnerships - WCG
Tanisha LaVeck - Clinical Research Financial Analyst - Holy Cross Health – Research Department
Geoffrey Schick - Director, Strategic Site Partnerships - WCG