The SCRI team is able to carry out monitoring of studies and provide guidance and support on compliance to regulatory frameworks to achieve good quality data.

SCRI provides Study Monitoring expertise including:

• Provide regular oversight and monitor data acquisition to ensure procedural integrity
• Monitor the quality of the data including source data verification (SDV), and liaise with Clinical Research Coordinators (CRCs) to rectify problems
• Provide training for all CRCs and other research support staff in research procedures for each study

The Study Monitoring expertise is offered as part of SCRI’s Research Operations Division. To learn more about SCRI’s Research Operations, please click here.

To engage SCRI’s Study Monitoring expertise, please click here if you are planning an Investigator initiated study, or click here for other studies.