Oracle Health Sciences Clinical Development (formerly Phase Forward) is a cloud‑based platform for designing, managing, and analyzing clinical trials. Below is a curated list of 20 alternative clinical‑trial software solutions that offer comparable EDC, CTMS, eTMF, and analytics capabilities.
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Comprehensive EDC and data management platform with built‑in risk‑based monitoring, analytics, and patient‑centric tools.
Regulated cloud solution for electronic data capture, trial management, and integrated eTMF, built on Veeva’s Vault platform.
User‑friendly, SaaS‑based EDC system focused on rapid study start‑up, mobile data capture, and real‑time monitoring.
Intuitive, GDPR‑compliant EDC with drag‑and‑drop study builder, automated validation, and API integrations.
Open‑source clinical trial platform offering EDC, CDMS, and data analytics with strong community support.
Secure, web‑based application for building and managing online surveys and databases, widely used in academic research.
Cloud‑based CTMS/EDC solution that integrates trial planning, patient recruitment, and real‑time analytics.
Decentralized clinical trial platform enabling remote patient monitoring, eConsent, and mobile data capture.
Modular CTMS/EDC suite with eTMF, safety, and pharmacovigilance modules, designed for CROs and pharma sponsors.
End‑to‑end clinical trial management system offering EDC, eTMF, randomization, and risk‑based monitoring.
Integrated clinical trial management system that connects study planning, site management, and financials.
Specialized electronic trial master file solution that integrates with Veeva Vault CDMS and other Veeva products.
Comprehensive suite covering EDC, eTMF, imaging, and site management with strong regulatory compliance.
Cloud‑based CTMS/EDC platform focused on simplifying study start‑up, monitoring, and reporting.
Modular EDC system with built‑in randomization, ePRO, and integration capabilities for sponsor‑centric workflows.
All‑in‑one clinical trial platform offering EDC, eTMF, patient engagement, and analytics in a single cloud environment.
Specialized eConsent solution that integrates with major EDC platforms to streamline patient enrollment and compliance.
Platform for clinical trial transparency, site payments, and regulatory document management, complementing existing CTMS/EDC.
Patient‑centric mobile platform for remote data capture, wearables integration, and real‑time safety monitoring.
Lightweight EDC focused on rapid deployment for early‑phase studies, with built‑in ePRO and audit‑ready reporting.