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.

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

eClinical is the next-generation self-configurable clinical trial workflow management solution site feasibility and selection, study start-up, training/certification, safety alert management, remote monitoring, patient recruitment and eTMF.

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.

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

MAISi is a user-friendly and sophisticated Clinical Trial Management System that has been designed to assist clinical research sites.

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.

Intrinsic Clinical Systems CTMS contains all of the features of a comprehensive, flexible clinical trial management system.

21 CFR Part 11 Compliant, Web-Enabled eClinical Suite with integrated Clinical Trial Management.

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

Cloudbyz CTMS solution is an innovative cloud-based software designed to streamline the clinical trial management process, enabling greater efficiency, faster time-to-market, and reduced costs.

EDGE is an innovative cloud-based research management system created by the Clinical Informatics Research Unit at the University of Southampton.

Patient pre-screening AI assistant for clinical trial recruitment.

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

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.

Clinical trial management system

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 softwar

Delve Health combines eCOA/ePRO, wearable device integration, real-time analytics, and Concierge-as-a-Service™ into one clinical trial execution platform. Designed for sponsors, CROs, and research sites running hybrid and decentralized studies, Delve achieves 92–98% ePRO completion rates through proactive patient outreach in 120+ languages, device compliance monitoring, signal quality control, and site burden reduction. Used across oncology, CNS, cardiovascular, rare disease, respiratory, and po

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