Conference, General Event

HCCA- Research and Compliance Conference

Posted By: Katie Regan / April 27, 2015

The Research and Compliance Conference will cover topics including: Auditing Clinical Research Billing: How Do You Know You Are Doing it Right?, Unified Compliance Framework: Establishing Risk Based Monitoring (RBM) for Clinical Research, Human Gene Transfer, Institutional Biosafety Committees, and Biological Materials Oversight: Past, Present and Future for Clinical Research, Billing and Compliance Concerns in Personalized Medicine, Keeping up with evolving clinical trial disclosure requirements – Is your institution prepared?, Compliance and Research Billing Considerations for Unique Clinical Research Trials, Conflict of Interest Management in an Academic Medical Center, Creation of a Clinical Trials Business Office: Operations and Compliance Considerations, and Lessons Learned, Cybersecurity of Medical Devices and Impact on Research, Designing Audit Ready Training Using FDA 483’s and Warning Letters, Research Year in Review, Embracing Quality:  One Institution’s Approach to Managing Compliance Risks, Enterprise Research Risk, Fair Market Value Issues/Commercial Reasonableness with Research Physicians, Focusing on the Management Plan: Managing Individual and Institutional Conflicts of Interest in Clinical Research, Is Sunshine the best medicine?  What research shows about managing conflicts of interest through disclosure, Process Improvement in Animal Research Compliance

About the Author: Katie Regan