Investigator Responsibilities in Clinical Trials: Practical Applications of Good Clinical Practices
This short course is targeted at principal investigators who are responsible for providing oversight and ensuring that Good Clinical Practices are followed in their research studies. Attendees will learn best practices for how to handle issues that arise in the daily conduct of research studies and how to handle these issues in compliance with GCP. Attendees will also hear examples presented by UNC investigators who are responsible for implementing GCP in their own research projects.
Event details
When
Dec 09, 2011
from 08:30 AM to 12:00 PM
from 08:30 AM to 12:00 PM
Where
Brinkhous-Bullitt Building, Room 219
Contact Name
Filed under:
CTSA
