ValidCare
Validcare is a US-based contract research organization (CRO) that provides cloud-based, regulatory-compliant clinical trial infrastructure and end-to-end operational services. The company offers a Platform-as-a-Service (PaaS) for site-based, hybrid and decentralized clinical studies, combining e-source data capture, trial management functionality, automated patient engagement, and real‑world evidence support to help sponsors plan and execute trials on time and on budget.
Industries
N/A
Products
Cloud-based clinical study platform (21 CFR Part 11 compliant)
A configurable clinical study platform supporting EDC, CTMS, eConsent, ePRO/eCOA, investigator portal and mobile patient apps for hybrid and decentralized trials.
Cloud-based clinical study platform (21 CFR Part 11 compliant)
A configurable clinical study platform supporting EDC, CTMS, eConsent, ePRO/eCOA, investigator portal and mobile patient apps for hybrid and decentralized trials.
Services
End-to-end CRO services
Protocol development, site/investigator selection, patient recruitment, monitoring, data management and regulatory support for interventional and non-interventional studies.
Platform-as-a-Service for hybrid and decentralized trials
Provision of a configurable, private-label clinical study platform that supports site-based, hybrid and decentralized studies with investigator and patient-facing apps.
Data management and statistical services
Centralized data cleaning, database lock support and statistical analysis to accelerate availability of the final dataset.
Real-world evidence study support
Design and operational execution for RWE and observational studies including regulatory intelligence integration.
White-label platform deployments
Private-labeling of the clinical study platform for partners and institutions.
End-to-end CRO services
Protocol development, site/investigator selection, patient recruitment, monitoring, data management and regulatory support for interventional and non-interventional studies.
Platform-as-a-Service for hybrid and decentralized trials
Provision of a configurable, private-label clinical study platform that supports site-based, hybrid and decentralized studies with investigator and patient-facing apps.
Data management and statistical services
Centralized data cleaning, database lock support and statistical analysis to accelerate availability of the final dataset.
Real-world evidence study support
Design and operational execution for RWE and observational studies including regulatory intelligence integration.
White-label platform deployments
Private-labeling of the clinical study platform for partners and institutions.
Expertise Areas
- Contract research organization (CRO) services
- Decentralized and hybrid clinical trials
- Clinical protocol development
- Clinical data management and eSource
Key Technologies
- Cloud-based clinical trial platform
- 21 CFR Part 11 compliance
- Electronic data capture (EDC)
- Clinical Trial Management System (CTMS)