Total Products under this Category: 222
Last updated: November 01, 2026
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Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialKit.
Underlying data: [Grid® JSON](https://www.g2.com/categories/clinical-trial-management-systems/grids.json?focus%5B%5D=oncore-ctms&focus%5B%5D=viedoc&focus%5B%5D=clinical-research-suite&focus%5B%5D=florence-healthcare-florence-ebinders&focus%5B%5D=rave-ctms&focus%5B%5D=clario-ctms&focus%5B%5D=vial-edc-esource&focus%5B%5D=trialkit)
All Cantab tests are simple to administer and show strong correlations to brain constructs and known deficits in various disorders, as well as high sensitivity to interventions and small changes over time.
Catchtrial EDC+ by Medigen Suite is a next-generation EDC software platform designed for modern clinical trials. It unifies electronic data capture, eCRF design, medical imaging (DICOM), risk-based monitoring, safety adjudication, analytics, and AI-driven insights into one secure, compliant environment. Built for sponsors, CROs, and research organizations, Catchtrial helps teams accelerate study execution, improve data quality, ensure regulatory compliance, and deliver approval-ready clinical evidence. The platform also supports ePRO, eCOA, eConsent, and decentralized trial capabilities for seamless clinical data capture across all study phases.
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Clinical Trial Management System is a complex platform to plan, track, and control R&D activities across trials, sites, and vendors. • Project planning, milestones, Gantt-style charts, risk and issue tracking. • Sites, investigators, and vendors management. • Training management. • Electronic documents workflows. • Dashboards and electronic reports for operational oversight and inspection readiness.
Chronicles eCRF is a configurable SaaS solution which may be set up by clients in strict compliance with the protocol in both interventional (Phase I-IV and BE/BA) studies and non-interventional programs. • Integrated randomization, stratification and blinding. • Built-in trial supply management tools. • Study-specific form builder with edit checks, lab ranges, and multi-language support. • MedDRA and ATC coding, CDISC/CDASH-ready datasets. • Compatibility with modern statistical software such as SAS, R, SPSS, Excel, etc.
A global solution for the electronic management of clinical trials EDC – IWRS – CTMS – CDMS – ePRO – IoTs – eTMF … CleanWEB is a secure Internet platform dedicated to managing national or international clinical electronic studies, registries and cohorts, mono or multi-centric. It is especially made for projects of all kinds: clinical trial from phase I to IV, real-life based studies, veterinary studies, epidemiological studies. Certifications : CDISC ODM – ISO 9001:2008 – 21 CFR Part 11 Compliance
Climedo’s mission is to bring the best treatment to every patient by empowering healthcare professionals with intelligent software solutions. Together with Europe’s leading hospitals, we have developed a cloud-based platform for cutting-edge clinical validation and post-market surveillance of medical devices and pharmaceutical products. By digitally connecting all stakeholders (Medical Device manufacturers, Pharma companies, CROs, hospitals and patients), Climedo allows for increased performance, better cost-efficiencies - and ultimately - accelerated medical innovation.
Average Rating: 4.2/5.0
Total Reviews: 3
Rating: 4.5/5.0 stars
— Callum C.
"Manage Post Market Surveillance activities "EDC""
Rating: 4.5/5.0 stars
— Ritesh B.
ClinBase is electronic medical records and prescription management software for independent medical practitioners in Mexico. Consultation notes use the PSOAP format with vital signs capture and become locked after a digital signature, ensuring an audit trail. Prescriptions are generated as legally valid PDFs, customizable with institutional emblems like UNAM and CONACEM. The system features CIE-10-based autocomplete for medications and diagnosis. Patients book appointments via links or QR codes without accounts, receiving automated email reminders with options to confirm or cancel. Cancellations update the calendar instantly, notifying the practitioner. An AI assistant transcribes consultations into PSOAP sections, and video consultations run directly on the platform without installation. Analytics track patient counts, consultation totals, and diagnosis trends. Patient data exports to Excel, PDF, and HL7 CDA formats, with AI-assisted migration from Excel files or paper records.
Clinevo Clinical Trial Management System (CTMS) is a cloud based, highly configurable, "end-to-end platform which" helps manage all aspects of clinical trials including : Site Monitoring Visits Milestones - Planning and Tracking Activities - Tasks & Deviations Payments - Site & Investigator Investigational Product (IP) Tracking & Inventory (IWRS) Patient Recruitment & Randomization (IWRS) Patient Visits - Scheduling and Tracking Site Selection, Site Initiation, Investigator Selection Master Data Management (Sites, Investigators) Regulatory documents & Compliance Tracking Study Budgets & Training Management Adverse Event Tracking and many more. Clinevo Clinical Trial Management System (CTMS) meets the regulatory guidelines including security, access control, change controls, audit trails, and the best system validation.
Clinical Trials for HubSpot and Salesforce integrates public clinical trial data into your CRM, adding unique search functions, reporting capabilities, and automation. No separate software, no downtime for a learning curve – just clean data that drives business.
Centralized software which provides ways to manage, track, and document throughout the clinical trials process.
