Benefits

- PROTOCOL ADHERENCE: Streamline protocol deviation management and enhance adherence with centralized tracking and easy generation of deviations.
- DATA QUALITY: Minimize data entry errors and ensure data integrity with real-time validation checks, audit trails, and data tracking.
- DATA COLLECTION: Reduce manual data entry errors, speed up data capture and analysis with automated EDC forms and customizable reporting.
- ACCESSIBILITY: Access RTMS seamlessly with a single login for all activities for users with eCRF access.
- REAL-TIME REPORTING: Get real-time insights into IMP status and location and prevent delays with automated low-stock notifications.
- RESOURCE MANAGEMENT: Streamline IMP distribution, optimize inventory, and ensure timely kit delivery with real-time tracking and task automation.
- ERROR REDUCTION: Reduce data entry errors and manual queries by up to 67%. Minimize reconciliation and ensure proper IMP allocation with integrated RTSM and eCRF.
- TIME SAVINGS: Enhance efficiency and accelerate trial management with interoperable tools and real-time reporting. Set up, deploy, and validate eCRFs in weeks, minimizing future issues and time needed to lock the database with data validation checks.
- COST SAVINGS: Save up to 67% of CRAs' time on query resolution, streamline EDC form development, and reduce labor costs by automatically allocating kits nearing expiration to prevent wastage.

Compliance With

- ICH GCP E6
- Good Clinical Data Management Practices, edition 4 (GCDMP)
- Good Automated Manufacturing Practice, edition 5 (GAMP 5)
- FDA 21 CFR Part 820
- FDA 21 CFR Part 11
- Declaration of Helsinki
- ISO 9001:2015 standard
- ISO 27001:2022 standard
- EudraLex, vol. 2 and 4
- GDPR, FADP, and HIPAA

The next step in advancing your clinical research is with us.