Products

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

**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

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

RealTime-Devana is a holistic business intelligence platform designed specifically for research site organizations, driving transparency and accountability across all functional groups. From pipeline management and streamlined study start-up through to historical trial metrics, Devana provides one source of truth for all your clinical trial data and processes. Improve turnaround times and stand out to CROs and sponsors with Devana’s powerful workflow improvements and data analytics.

Clinical trial management system

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.

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

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

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

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.

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

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

Aurea Compliance Manager delivers end-to-end integrated solutions designed to address the specific workflow and compliance needs in the Life Sciences.

Trial Interactive provides a practical, author-to-archive approach for streamlining clinical operations, reducing risk, and expediting time-to-market. Clinical professionals around the world consistently choose Trial Interactive as their preferred document management and oversight platform

ConciergeTMF is an innovative Software-as-a-Service (SaaS) provider specializing in Research and Development (R&D) archival management. Their unique approach transcends traditional software solutions by offering a comprehensive platform that seamlessly blends technology and human expertise. Key features of ConciergeTMF's platform include: Human-in-the-Loop Intelligence: At the core of ConciergeTMF's offering is the fusion of AI technology with human oversight. This synergy ensures that doc

Cloudbyz eTMF provides a user-friendly solution that simplifies the complex process of access, retention, and retrieval of clinical trial documents, while ensuring that compliance requirements are fully met.

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