How to Improve Your Site Compliance and Performance
Every member of the research team is committed to compliance. However, administrative headaches and staffing shortages can increase risks of non-compliance at the site level. Sites are busy conducting their non-trial clinical patient care, so it’s challenging to stay on top of all regulatory and activation requirements when they are not supported well. This eBook will examine sites and protocol violations and discuss ways you can help your sites to be more compliant without imposing additional burden impacting critical timelines.
In this guide, we:
- Break down the most common site violations, and reasons for protocol deviation
- Discuss tactics and strategies to help your site team overcome these common challenges
Download our eBook to learn more.
DATE
Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour