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.
Centralized software which provides ways to manage, track, and document throughout the clinical trials process.
eClinDirect, DSG’s web-based CTMS, is a project management application that helps you to capture and share a wide variety of clinical trial project status information across multiple studies.
Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, global cloud platform with a flexible suite of tools that allows sponsors, patients, providers & CRO's to work together as a team in clinical trials. Our solutions enable more efficient clinical research, more effective healthcare delivery, and more accurate precision and predictive medicine. Our vision is to accelerate the path to human discovery and medical cures. We are passionate about driving
Curebase is the modern eClinical platform built for flexibility, usability, and full-study oversight, empowering sponsors, CROs, and sites to launch faster, adapt confidently, and deliver better participant experiences with next-gen ePRO, eConsent, engagement tools, and integrated EDC.
Smart Omix by Sharecare is a software platform enabling researchers to design, launch, manage, and analyze real-world digital clinical studies at scale. Researchers across the healthcare and life sciences industry can leverage our self-service platform or concierge study- building services to conduct rigorous, high- quality, real-world data collection via the Smart Omix app (available on iOS and Android). Using our first-of-its-kind SaaS model, researchers can include rich data into studies to g
An innovative, no-code platform for conducting participant-centric digital clinical trials in record time. Collect eConsent, ePROs, and wearable device data from Fitbit, Garmin, Oura, Apple Watch, Google Fit and more. Connect to EHR and claims records for a more robust longitudinal record of each participant. All data is stored in the HIPAA-compliant, Meaningful Use Certified EDC HIEBus™ platform, and is then exported to researchers in an easy-to-use format, allowing scientists to focus on sc
Health Studio is a clinical data platform built exclusively on Google Cloud. This low code platform allows organizations to build AI-enabled clinical solutions in a fraction of the time, unlocking all Google cloud resources and APIs with clicks not code. This allows organizations to introduce AI-enabled workflows and agent based applications with lower risk and cost and accelerate the time to realize the benefits. Further Health Studio's modular and customizable design integrates with existing t
Wemedoo’s oomnia system integrates powerful tools including CTMS, EDC, eTMF, ePRO, eCOA, eConsent, eSource, and RTSM, enabling end-to-end oversight and seamless collaboration across the clinical trial lifecycle.
Patient pre-screening AI assistant for clinical trial recruitment.
With our strong continuation capabilities, Taimei Technology CTMS (eCooperate) can seamlessly integrate into your existing processes and workflows, allowing you to customize the system to fit your unique needs. Whether you're managing a single-site study or a complex, multi-site trial, our platform can be tailored to your specific requirements.
SUMMA™ is a configurable solution that allows researchers to generate new insights by integrating large disparate real-world data sources such as electronic health records (EHR), historical clinical trails data, EDC, eCOA, ePRO’s, claims data, disease registries, labs, medical devices, wearables, and Health IOT.
Syncora is a cloud-based platform revolutionizing study startups for CROs, sponsors, and investigative sites. Born from relentless innovation, it automates workflows, captures and displays real-time data, and empowers teams to navigate complex startup processes with speed and precision. With a user-friendly interface, secure cloud backup, and a commitment to transparency, Syncora ensures timelines are met, delays are addressed proactively, and clinical trial operations run seamlessly from day on
Agentic AI Assistant Clinion’s Agentic AI Assistant changes how teams interact with clinical trial data. Users can simply ask questions and get instant answers drawn directly from study data, protocol context, and operational workflows, instead of navigating through complex datasets. Powered by a system of specialized agents, it interprets intent, connects it to the right data source, and delivers responses that are grounded, traceable, and ready to use. What can you expect? ● Ask questions,
Clinion eConsent replaces manual consent processes with a digital system designed to improve patient onboarding and ensure compliance. Built within a unified platform, it enables real-time tracking, secure documentation, and seamless integration with Clinion EDC. What can you expect? ● Flexible Consent Models Support site-based, remote, and ePRO-linked consent workflows based on study needs. ● Faster Patient Enrollment Reduce onboarding timelines with digital consent and automated re-consenting
An application for managing expanded access and compassionate use programs — covering request intake, medical review, ethics approval, regulatory filing, and logistics coordination.
Medigen® CTMS+ centralizes planning, monitoring, document management, product oversight and finances to streamline trials, reduce costs, and deliver faster, smarter results.
Scienta Lab is an AI-powered platform pioneering Precision Immunology