We have everything you need to achieve process excellence, from the most up-to-date knowledge of regulatory requirements and evolving committee best practices to industry-leading technologies. Access Unmatched Experience Our staff has over 200 years of combined experience in clinical trials to measurabl...
WCG’s robust and user-friendly clinical trial platform offers end-to-end training, adverse event safety reporting, and regulatory document exchange with one login.
Is an institution that is serving as a data coordinating center subject to the same IRB requirements as the sites that are implementing the clinical research that produces the data? Existing OHRP guidance provides some relief. However, a large gray area remains. SACHRP will be examining the ...
Clear, timely communication before new projects – and accountability and transparency throughout – ensure understanding and agreement on expectations and availability requirements. Optimize (& Likely Reduce) Costs Our streamlined approach to DMC support hits the fast-forward button on member recruitment ...
It’s user-friendly with simple tracking and monitoring of raters and allows sites to ensure they’re meeting their site activation requirements in a timely manner. In addition, the WCG team has been extremely collaborative in providing clinical recommendations for the development of rater ...
and certifying raters. It’s user-friendly with simple tracking and monitoring of raters and allows sites to ensure they’re meeting their site activation requirements in a timely manner. In addition, the WCG team has been extremely collaborative in providing clinical recommendations for the developme...