Lorrie Divers, President, QRCP Solutions, Inc. will present 'Multi-Site Study Oversight: Investigator Responsibilities, Quality by Design, and Risk Management'.

This virtual presentation will discuss clinical trial Sponsor-Investigator responsibilities from both a regulatory and institutional perspective. The principles of Quality by Design and risk mitigation will be introduced with practical applications and case studies supporting their application to multi-site study oversight by a UR Principal Investigator.

Learning objectives:
1. Describe the regulatory obligations of clinical trial Sponsor-Investigators.
2. Describe the principles of Quality by Design and risk mitigation as these apply to clinical trials.
3. Demonstrate the ability to apply the principles to their clinical trial role/responsibilities.

Register: https://rochester.zoom.us/webinar/register/WN_PpludMIvRQKXFvx5lck4GQ#/registration