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.

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,

Secure portal for central readers, KOLs, and investigators to review and share data and documents. • Built-in DICOM anonymization, centralized imaging assessment (MRI/CT), and remote monitoring. • Controlled reviewer access. • eCRF-like report forms. • Collaboration tools to support central review processes.

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

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.

Catchtrial® eConsent enables participants to review and sign informed consent from anywhere using telemedicine-inspired technology. Compatible with Android and iOS, it removes the need for on-site visits and provides a seamless, mobile-first experience for patients.

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

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

adWATCH - AE helps pharmaceutical organizations manage and report adverse events that occur during clinical trials.

LAStools is a software suite to classify, tile, convert, filter, raster, triangulate, contour, clip, and polygonize LiDAR data.

Launching a new category of pre-clinical research with AI-driven insights from functional human organs in 'Human Data Trials'.

The only solution to offer collaborative trial prep, live transcription, deposition management and customizable presentation in a single online platform.

Ofni Clinical is a clinical data management tool that rapidly creates and implements secure, regulatory compliant clinical trial databases.

Suite of modules that assist in clinical trials through data input, management, consent forms, and electronic data capture forms.

Redefine clinical trial regulatory document and TMF management with an automated, customizable 21 CFR Part 11 compliant solution.

Help your Clinical Operations team continuously improve speed, efficiency and data quality across your portfolio of clinical trials

A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM.

Leapcure provides patient recruitment services to pharmaceutical companies to help accelerate clinical trials with the voices of all stakeholders at the center.

An application for managing corporate ethics programs — including whistleblower intake, complaint triage, investigation workflows, and compliance culture measurement.