Cros

Ensure safe transport of investigational products with meticulous planning and rigorous procedures to mitigate hazards and uphold biosafety.

Federal requirements have shifted to require most multisite clinical trials to rely on a single IRB (sIRB) for trial oversight.

Learn practical strategies on how to improve diversity in clinical trials for historically under-represented groups.

Sponsors are uncertain about how to design a DCT to ensure efficient performance delivery, learn how to set your organization up for success.

Each incidental finding has an impact on how research professionals handle the result and whether it should be shared with participants.