Interactive Web Response Systems (IWRS)
OCT is happy to offer Interactive Web Response Systems (IWRS) for your clinical trials. This is a part of OCT EDC system. At OCT we use a self-own developed Clinical Data Management Platform – OCT CDMS. The system is fully compliant to 21 CFR Part 11, FDA Guidelines for Computerized Systems used in Clinical Trials, European Regulations, etc. OCT CDMS is compatible to CDISC ODM and CDASH standards.
Once installed the Interactive Web Response Systems is available 24/7 for use by sites, study participants and project team members.
All study specific transactions are recorded into a study-specific database, and information can be exported into custom reports.
Live technical support is available to sites and study participants via web access.
IWRS services include:
Our expert team of statisticians and programmers can develop algorithms to suit the needs of data management for clinical trials. The system automatically provides real-time confirmation of randomization activity.
The IWRS authenticates each caller. User IDs and passwords are assigned and securely distributed upon site activation. As standard procedure for clinical trials management at OCT, all databases, files and programs are backed up and sent to secure storage as part of disaster recovery measures. At OCT you can feel secure.