Products

Intrinsic Clinical Systems CTMS contains all of the features of a comprehensive, flexible clinical trial management system.

Centralized software which provides ways to manage, track, and document throughout the clinical trials process.

Protocol Manager helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.

Clinion's Clinical Trial Management Software (CTMS) gives enhanced visibility into all aspects of the clinical trial process - from study plan, Remote monitoring, and Clinical data management.

Trialflare is the flexible platform for getting accurate research data. Trialflare is a platform that allows researchers and people involved in R&D activity to collect meaningful data from participants as part of a controlled trial or survey. It is used across the cosmetics, health, and supplements space to help organisations understand the effect of a product or development. Whilst being a security-focused product, Trialflare is also easy to use for researchers and participants alik

Studylog is in-vivo study management software used by pharmaceutical companies, biotech firms, contract research organizations (CROs), and academic research institutions to manage the workflow of in-vivo research studies. The platform covers the study lifecycle from design through reporting, including study design and scheduling, task and measurement tracking, data acquisition, randomization, data analysis, and report generation. The software is used to replace spreadsheet-based tracking method

**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

Centralized Monitoring Built for Modern Clinical Trials Improve trial performance by up to 30% with monitoring that reduces complexity and keeps your study on track. Focus on what matters most • Vizualize changes over time instantly • Quickly identify critical risks by uncovering hidden insights • Minimize wasted effort by directing attention where it’s needed Confidence in every decision • Full visibility with intelligent, dynamic data structures • Adapt easily to emerging needs and regulatory

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.

With a real-time view across clinical trial processes, Vault CTMS improves operational efficiency, streamlines collaboration, and enables faster, higher-quality trial execution.

A Comprehensive Solution to Capture and Manage Clinical Trial Information. The Ennov Clinical suite consists of Clinical Data Management applications (EDC, RTSM and ePRO) as well as Clinical Trial Management applications (CTMS and eTMF) that are available for deployment in the cloud or on premises

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

Patient pre-screening AI assistant for clinical trial recruitment.

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

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.

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

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

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