Total Products under this Category: 182
Last updated: September 06, 2026
Why You Can Trust G2's Software Rankings:
G2's software rankings are built on verified user reviews, rigorous moderation, and a consistent research methodology maintained by a team of analysts and data experts. Each product is measured using the same transparent criteria, with no paid placement or vendor influence. While reviews reflect real user experiences, which can be subjective, they offer valuable insight into how software performs in the hands of professionals. Together, these inputs power the G2 Score, a standardized way to compare tools within every category.
Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialHub.
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=trialhub)
Intrinsic Clinical Systems CTMS contains all of the features of a comprehensive, flexible clinical trial management system.
Set of modules that help all stakeholders effectively manage all areas of clinical and research management.
Jeeva eClinical cloud helps clinical researchers, patient advocacy groups, clinical research organizations (CROs), public health research organizations, and Biopharmaceutical sponsors to accelerate remote patient recruitment by 3x faster by reducing the logistical burdens on patients and study teams by over 70%. This modular software design allows a rapid study configuration with the features and workflows that fit the specific trial protocol whether short-term or long-term, cross-sectional or longitudinal, interventional or observational studies.
ArisGlobal’s LifeSphere platform is a suite of unified cloud solutions that helps hundreds of global life sciences companies accelerate development, maintain compliance and streamline collaboration between cross-functional teams. LifeSphere enables the life sciences industry to bring safer products to market more quickly.
The Magana Trial Manager is an intuitive software solution for conducting clinical trials. This validated software is designed for CROs, pharmaceutical, IVD and medical device manufacturers (e.g. for CE marking, FDA submission or PMCF according to MDR/IVDR) and academic researchers. The core functionality is the eCRF/EDC - from design through clinical data collection in the study to completion, export and archiving of data. The system supports multilingual studies, different end devices (mobile/tablet/computer), automatic input validation, electronic signatures, role-based access control, and much more. Customers can book exactly the modules they need for their particular study. E.g. multi-center support, query management, biosample management, eSurveys/ePRO, or paper CRF support (print, scan, semi-automated data capture, validation).
MAISi is a user-friendly and sophisticated Clinical Trial Management System that has been designed to assist clinical research sites.
Maptrial CTMS+ is a clinical trial management system by Medigen Suite that centralizes planning, monitoring, document management, product oversight, and financial tracking to streamline trial operations. The trial management software integrates eTMF, risk-based monitoring, site payment processing, MedDRA coding, and product tracking into a single governance platform — helping sponsors, CROs, and research organizations reduce costs and deliver faster, smarter results across multi-site studies.
At Medable, we believe health and access to clinical trials is a human right, and participation should be easy. We understand that inclusive medicine removes barriers to clinical trials creating new trial efficiencies that amplify science, enabling you to bring treatments to market faster than ever before. Amplify science with the No. 1 rated leader in DCT Rated #1 DCT Provider by Everest’s PEAK Matrix® Assessment 2021 Extensible Platform Built to securely scale your studies today or in the future with a unified modern cloud infrastructure and flexible modular apps. Patient-Centric Services Put the patient at the center of care. With a range of DtP services including home health nursing, Connected Devices and Remote Sites, make participating in a trial as convenient as possible. Smart Data for Better Decisions Seamlessly integrates with hundreds of external data sources across: IRT, EDC, CTMS, EMR, Labs, Sensors, Wearables, Custom Systems, etc. Trusted DCT Ecosystem The largest and most trusted ecosystem of DCT partners including: CROs, System Integrators, Data & Tech, Devices - provide access to the smartest path forward for your organization and studies as they scale. DCT Training & Expertise The easiest way to increase your organization’s DCT expertise and start-up your studies efficiently. The Medable Platform Ecosystem Simplify the trial experience with a platform purpose built by clinicians, patient advocates, and technology experts. Because our platform is built from the ground up, not stitched together, we’re able to offer an intuitive experience for all stakeholders that integrates with any eClinical system and delivers real-time data insights for monitoring, safety, and efficacy.
Medigen Suite is Meditrial's eClinical platform for streamlined global clinical operations. Designed as a modular clinical trial software, it supports medical device companies, biotechnology firms, pharmaceutical sponsors, CROs, and academic research institutions across all study phases. - Catchtrial EDC delivers comprehensive electronic data capture with ePRO, eDiary, eConsent, and decentralized trial (DCT) capabilities for seamless patient engagement and remote data collection. - Maptrial CTMS provides full clinical trial management, including site monitoring, study tracking, and operational oversight for efficient trial execution. - Mastertrial LMS+ delivers scalable digital training for investigators and research teams to accelerate site activation and ensure regulatory compliance. Medigen Suite also offers a lightweight, cost-effective configuration for rapid study startup and feasibility assessments, making it accessible for organizations of any size.
CDISC-based fast eCRF production with AI technology. Provides customized EDCs. GAMP5 certification as an integrated platform for clinical trial data management. 21 CFR Part 11, Annex 11 Certification ISO900:2015 Certification 24/7 Global Service Support Team Quick trial start and affordability compared to other systems
