Thoroughly and efficiently incorporating the complexities of human research protection involves more than just risk mitigation, making it one of the most challenging aspects of conducting a clinical trial. 

Use CTTI’s recommendations and resources for protecting participants in clinical research to streamline, improve transparency, and enhance communication in your trial. 

Projects

SINGLE IRB

Adopt a single IRBs (sIRBs) for multicenter clinical trials in an effort to streamline and optimize study execution.

INFORMED CONSENT

Optimize your informed consent process and provide participants with clear, accurate information about trial specifics, risks, and benefits. 

SAFETY REPORTING

Improve the quality and efficiency of safety reporting, reduce irrelevant reports, and increase adherance to FDA requirements for clinical trials conducted under an IND.

DATA MONITORING COMMITTEES

Enhance your partnership and communication with DMCs, better understand the role of the DMC, and learn about best practices for DMC conduct, composition, and training.