Clinical Trial Monitoring

We have extensive experience in monitoring clinical trials. Clinical Trial Associates (CRAs) work according to the standards of Good Clinical Practice (ICH GP), study specific procedures as well as study sponsor’s Standard Operating Procedures (SOPs). The team has working knowledge in handling e-systems like Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), Interactive Voice Response Systems (IVRS) and Interactive Web Response Systems (IWRS). Each Clinical Research Associate is responsible for site and site staff oversight and management, study team training and meeting the timelines set for the study milestones at the site.