Products

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

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.

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

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

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

inTrial Manage is the operating system for plaintiff trial firms. We replace the fragmented stack most firms duct-tape together — case management, client intake, eSign, e-fax, texting, team chat, and document storage — with one purpose-built platform. AI handles the work that used to eat your team's day: medical chronologies built in seconds, demand letters drafted from your case file, complaints generated on command. Built by plaintiff lawyers who were tired of paying for software that was neve

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 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.

Medigen® CTMS+ centralizes planning, monitoring, document management, product oversight and finances to streamline trials, reduce costs, and deliver faster, smarter results.

Trially is the first AI-native clinical trial platform that matches, engages and enrolls patients at breakthrough speed and ~95% accuracy. Loved by customers, Trially LLM agents fill trials faster—with 2-6x increase in enrollment rate, 73% fewer screen fails, and 91% less prescreening time. Trially’s site-based software rapidly prescreens patients from any clinical data source, fully compliant with HIPAA, SOC 2, FDA 21 CFR Part 11, and ISO 27001. Designed to meet the needs of Physicians, Site

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

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

Scienta Lab is an AI-powered platform pioneering Precision Immunology

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

**HEKMA.ai** is an AI-powered clinical intelligence platform transforming how patients, healthcare providers, researchers, and life sciences organizations connect with clinical research. By combining intelligent patient matching, secure healthcare data integration, and advanced analytics, HEKMA.ai accelerates clinical trial recruitment, streamlines research workflows, and improves access to life-changing treatments. Committed to innovation, security, and inclusivity, HEKMA.ai is helping shape a

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.

Catchtrial® EDC+ is a next-generation clinical trial platform combining data capture, imaging, safety workflows, and AI-driven analytics in one integrated, secure environment. It enables real-time oversight, faster decision-making, and the delivery of high-quality, approval-ready data across global studies. Catchtrial® EDC+ serves as an intelligent clinical trial governance environment, where investigators, core labs, safety adjudication teams, monitors, and statisticians collaborate around r