Clincase is a cloud‑based Clinical Trial Management System (CTMS) that helps sponsors plan studies, manage sites, track enrollment, and capture data. The following 20 platforms provide comparable or expanded capabilities for running clinical research, ranging from full‑stack CTMS solutions to lightweight electronic data capture (EDC) tools.
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Enterprise‑grade CTMS with integrated eTMF, site management, and real‑time analytics, built on Veeva’s life‑sciences cloud.
Comprehensive eClinical platform offering CTMS, EDC, randomization, and risk‑based monitoring for large‑scale trials.
Robust CTMS and EDC suite with advanced analytics, adaptive trial design, and seamless integration with Oracle Cloud.
Cloud‑native platform that combines CTMS, EDC, and patient‑centric tools powered by AI and Watson Health.
User‑friendly, SaaS‑based EDC and ePRO solution with built‑in CTMS features for fast study start‑up.
Intuitive, GDPR‑compliant EDC platform offering study builder, randomization, and lightweight CTMS capabilities.
Open‑source and commercial EDC/CTMS platform with flexible study design, audit trails, and extensive API integrations.
Free, secure web application for building and managing online surveys and databases, widely used for academic trials.
Mobile‑first eClinical platform delivering decentralized trial capabilities, eConsent, ePRO, and integrated CTMS.
Full‑featured CTMS with eTMF, site monitoring, budgeting, and regulatory document management.
Suite that combines CTMS, EDC, imaging, and patient engagement tools for complex therapeutic areas.
Cloud‑based CTMS focused on operational efficiency, risk‑based monitoring, and real‑time KPI dashboards.
Affordable, web‑based EDC/CTMS platform with built‑in randomization, eConsent, and audit‑ready reporting.
Integrated quality‑management and CTMS solution that links SOPs, training, and document control to trial operations.
Patient‑centric platform enabling decentralized trials, eConsent, ePRO, and a lightweight CTMS for rapid recruitment.
eConsent, ePRO, and patient engagement suite that integrates with existing CTMS for decentralized study workflows.
Modular CTMS offering study planning, site management, budgeting, and compliance tracking for mid‑size sponsors.
Compliance‑focused platform that adds transparency, registration, and results reporting to any CTMS.
All‑in‑one EDC/CTMS solution with eConsent, ePRO, and integrated patient portal for small to midsize studies.
Cloud‑based CTMS with built‑in risk‑based monitoring, budgeting, and real‑time data visualization dashboards.