Products

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

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

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

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.

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.

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

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.

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

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

RunSensible is a complete case management system for legal practices. It offers all the necessary resources to enhance organizational efficiency and expand operational capacity. With unlimited document storage and remote case data access, RunSensible is the ultimate central hub for case management, including documents, schedules, emails, assignments, and invoices, all in one place. It simplifies the management of cases, contacts, billing, calendars, and more.

OpenNova Software provides flexible and highly customizable payment solutions for big and small Payment Service Providers (PSP) worldwide.

A leading Clinical Trial Knowledge Platform, offering a transformative collaboration channel and clinical trial oversight.

PhlexTMF is an advanced electronic Trial Master File (eTMF solution designed to ensure the completeness, timeliness, and accuracy of clinical trial documentation throughout the study lifecycle. Developed by Phlexglobal, a recognized authority in TMF best practices, PhlexTMF integrates cutting-edge artificial intelligence to enhance document management efficiency and reduce inspection risks. Key Features and Functionality: - AI-Assisted Document Management: Utilizes pre-trained AI to prevent mi

SureETMF is a cloud-based electronic Trial Master File solution designed to streamline the management of clinical trial documents and data. It enables biotechnology and pharmaceutical organizations to capture, collect, share, view, digitally sign, store, and manage documents, medical images, videos, clinical trial data, and other electronic content essential for medical research. Key Features and Functionality: - Comprehensive Document Management: Facilitates the organization and retrieval of

ComplyDocs eTMF is an electronic Trial Master File (eTMF solution designed to digitize and streamline the management of essential clinical trial documents. By transitioning from traditional paper-based systems to a digital platform, ComplyDocs eTMF enhances the efficiency, accessibility, and compliance of clinical trial documentation processes. Key Features and Functionality: - Digital Document Management: Enables the electronic capture, organization, and storage of all essential clinical tria

LifeSphere eTMF is an advanced electronic Trial Master File system designed to enhance collaboration and efficiency in clinical research. By supporting the TMF Reference Model standard document types and the eTMF Exchange Mechanism Standard, it enables seamless, real-time file sharing among sponsors, CROs, and clinical sites. This ensures that all stakeholders can contribute to the Trial Master File as a single source of truth, leading to higher quality, more complete, and timely documentation.

Octalsoft's Electronic Trial Master File system is a comprehensive solution designed to electronically capture, organize, share, and store essential documents, images, and artifacts generated throughout the lifecycle of regulated clinical trials. By implementing a recognized taxonomy and structure, the eTMF system ensures efficient content management with built-in checklists and milestone tracking features. Key Features and Functionality: - Configurable TMF: A flexible, wizard-driven process