Products

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.

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

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.

Your Research Clinical Trial Management System (CTMS) is tailored to streamline trials, prioritising patient-centricity and process efficiency. Key features include protocol-driven automation for time-saving and accurate data input. Patient experiences are enhanced through digitalisation, optimising in-person tasks, visit bookings, and eConsent with a focus on improving retention. Predict future events by tracking historical metrics. Access user-friendly 'pay per play' eCOA modules, such as ePRO

Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.

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.

SimpleTrials is a Clinical Trial Management System for Sponsors, CROs and Sites. SimpleCTMS was designed and developed to offer the benefits of a CTMS (Clinical Trial Management System) without the extensive upfront financial and resource commitments associated with traditional enterprise systems or the inherent inefficiencies of worksheet trackers.

Ddots allows users to track adherence to protocol requirements each and every step of the way from patient treatment plans to required regulatory notifications.

Clinion's Clinical Trial Management Software (CTMS) gives enhanced visibility into all aspects of the clinical trial process - from study plan, Remote monitoring, and Clinical data management.

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

Clinevo Clinical Trial Management System (CTMS) is a cloud-based, highly configurable, end-to-end platform that helps manage all aspects of clinical trials. It meets all the regulatory guidelines including security, access control, change controls, audit trails, and system validation.

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/

Evado OnDemand is a cloud-based clinical trial management platform designed to streamline the setup and execution of clinical trials, studies, and registries. Developed and hosted in Australia, it offers a fully integrated environment that allows sponsors to run multiple trials across various sites efficiently. The platform is accessible via standard web browsers and mobile devices, ensuring flexibility and ease of use. Key Features: - Scalability: Supports an unlimited number of trials and s

Trialflare is the flexible platform for getting accurate research data. Trialflare is a platform that allows researchers and people involved in R&D activity to collect meaningful data from participants as part of a controlled trial or survey. It is used across the cosmetics, health, and supplements space to help organisations understand the effect of a product or development. Whilst being a security-focused product, Trialflare is also easy to use for researchers and participants alik

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

Intelligent Engineering for Clinical Trial Management Improve management and oversight of your clinical trials. Engility® supports rapid implementation and evolution with a highly intuitive user interface to increase adoption. Engineered for change, our continuous validation model enables your agility and journey towards unified trial governance.

SimpleTrials is the industry’s first on-demand, subscription-based CTMS for sites, vendors and sponsors. SimpleTrials CTMS provides the robust functionality needed to manage the most complex studies with the ease of use that busy teams require.

InfoEd Clinical Trials Software links trials to related protocols, grants, contracts, publications, conflict of interest information, and patents with a true clinical trial document management system. Accessible at any time, from any computer with Internet access, InfoEd’s Clinical Trials software and Clinical Trials Management System reduces administrative burdens and workloads with clinical data software by consolidating information in a single location that facilitates collaboration between a

A Comprehensive Solution to Capture and Manage Clinical Trial Information. The Ennov Clinical suite consists of Clinical Data Management applications (EDC, RTSM and ePRO) as well as Clinical Trial Management applications (CTMS and eTMF) that are available for deployment in the cloud or on premises