Products

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

Trialytix is the first software that covers all essential budget and cost operations of your clinical trial project.

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

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.

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.

Sarjen offers three specialized solutions for clinical trial management and lab automation. The Early Phase CTMS (BizNET) and Late Phase CTMS (Smart Trial Suite) are clinical trial management systems that streamline and automate early and late-phase trials, respectively. They ensure compliance, enhance data integrity, and reduce operational costs through features like intelligent automation and seamless integration. The Bioanalytical LIMS is a lab information management system that automates wor

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

Clinical trial management system

Medigen Suite offers a premier collection of intuitive clinical research solutions designed to streamline complex clinical trials. Their products include Electronic Data Capture, Clinical Trial Management Systems, and ePRO/eCOA applications, catering to various trial phases and sizes. The company targets organizations involved in clinical research, providing accessible and reliable cloud-based tools to enhance trial efficiency. With a focus on transforming the research experience, Medigen Suite

Clinical Trials for HubSpot and Salesforce integrates public clinical trial data into your CRM, adding unique search functions, reporting capabilities, and automation. No separate software, no downtime for a learning curve – just clean data that drives business.

ImproWise is your all-in-one, 100% web-based, secure, and HIPAA-compliant solution for Clinical Trial Management (CTMS) and Clinical Data Management (CDMS). Designed for flexibility, speed, and security, ImproWise integrates CTMS, CDMS, EDC, CTBM, CTPM, eTMF, ePRO, and RBACS functionalities, enabling rapid study setup, seamless multi-trial and multi-site management, and effortless customization. Our feature-rich and scalable platform caters to every stakeholder in clinical trials—from sponsors a

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

Scienta Lab is an AI-powered platform pioneering Precision Immunology

Hipp Health offers an AI-native platform that streamlines and automates behavioral health practice management operations.

Folio3 Digital Health's Clinical Trial Management Software (CTMS) revolutionizes clinical research by streamlining every phase from protocol design and site selection to patient recruitment, data collection, and regulatory reporting. Tailored for pharmaceutical firms, CROs, and research institutions, this cloud-based platform from Folio3 ensures seamless collaboration, real-time analytics, and automated workflows that enhance compliance with FDA, HIPAA, and GCP standards while slashing trial tim

An application for managing clinical trial registry submissions and results posting — supporting ClinicalTrials.gov, EU CTR, and other registries with deadline tracking.

An application for managing expanded access and compassionate use programs — covering request intake, medical review, ethics approval, regulatory filing, and logistics coordination.

UpSite Clinical offers TrialPro, an AI-enabled clinical trial budgeting software designed to assist research sites, sponsors and CROs in creating and negotiating study budgets and Medicare coverage analysis. The tool uses Fair Market Value benchmarks and automates various budgeting processes to ensure that sites avoid unpaid work and save time. Built by industry veterans, TrialPro analyzes protocols and generates budget grids while identifying unbudgeted work and generating coverage analysis. Th

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