Alternatives to QMENTA
Compare QMENTA alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to QMENTA in 2026. Compare features, ratings, user reviews, pricing, and more from QMENTA competitors and alternatives in order to make an informed decision for your business.
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Imorgon
Imorgon Medical
Significantly boost the speed and quality of your radiology reporting by eliminating manual data entry and reducing dictation for ultrasound and DEXA exams. Imorgon automates the transfer of modality measurements directly into Powerscribe, Fluency, or RadAI merge fields/tokens, ensuring unparalleled accuracy and consistency. Our specialized services guarantee - All measurements are seamlessly transferred - usually through DICOM SR - Electronic worksheets capture findings for direct insertion into your reporting system, replacing tedious dictation - Worksheets with integrated priors, calculators, and clinical decision support (TI-RADS, O-RADS, etc) - Integration with Epic and other EHRs - Vendor neutral - Dedicated support to ensure continuous operation. Experience a rapid ROI through drastically improved reporting overhead, making Imorgon the top ultrasound software choice for modern radiology departments aiming for peak productivity. -
2
ProtonPACS
Radsource
ProtonPACS is a picture archiving and communication solution that manages image access, storage and distribution, optimizing workflow across the organization. It includes front & back end patient management solutions that minimize manual and/or duplicate entry of patient information. HL7 integration to information systems (EHR, RIS, etc.) is included in the platform. ProtonPACS features Intelerad's Inteleviewer, a diagnostic viewer that provides radiologists and other healthcare professionals tools to optimize images, change layouts, measure critical data points, perform image reconstructions and create key images. In radiology environments, its worklist and integrated speech recognition engine allow radiologists to generate reports for referring physicians, and both reports & images are available via any web-enabled device through the system’s referring physician portal. ProtonPACS utilizes a secure hybrid model that employs on-premise hardware with simultaneous cloud hosting.Starting Price: $2/study -
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STARLIMS
STARLIMS
We simplify the complexity of your entire product lifecycle management process. Easy-to-use and adaptable to your organization’s needs, the STARLIMS brand of lab informatics solutions support the rapidly changing data management needs across your organization. Our laboratory information management solutions (LIMS software) can integrate with your current systems, while also identifying opportunities to improve processes so you can bring high quality and safe products to market faster. -
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Flywheel
Flywheel
Flywheel is the pioneering medical imaging data and AI platform powering healthcare innovation through streamlined data aggregation, curation and management. By leveraging cloud scalability and automating workflows, Flywheel helps organizations turn complex imaging data into analysis-ready datasets for accelerated research and AI development. Flywheel offers comprehensive solutions for pharma companies, providers, payors, system integrators, AI developers and academic medical centers. Leading scientists and researchers turn to Flywheel to accelerate their work and collaborate with ease. Our medical imaging AI platform streamlines the massive tasks of data discovery, aggregation, and curation; automates research workflows; and scales on demand. -
5
InsiteOne
InsiteOne
InsiteOne is a comprehensive enterprise imaging platform that consolidates medical imaging, data management, and diagnostic workflows into a unified, cloud-enabled system. It provides a vendor-neutral archive that stores imaging and clinical data from radiology, cardiology, pathology, and other departments, supporting standards such as DICOM, FHIR, and IHE for seamless interoperability. Whether deployed on-premises, in public or private cloud, or as a hybrid solution, the system enables centralized storage, automated lifecycle management, metadata enrichment, encrypted data protection, and geographically redundant disaster recovery, safeguarding billions of clinical images and patient records. Beyond storage, InsiteOne offers enterprise-wide imaging viewing; clinicians can access diagnostic images via a zero-footprint browser-based viewer (on desktop, tablet, or mobile) to perform measurements, 3D volume rendering, and advanced review, all without needing a specialized workstation. -
6
Saama
Saama
Actionable insights, driven by the industry's #1 AI-powered clinical analytics platform, enable your teams to manage risk and improve performance across studies, systems, sites, and vendors. State-of-the-art clintech from Saama is designed to streamline your workflows, automate time-consuming processes, and improve collaboration across clinical operations, medical review, data management, biostatistics, and pharmacovigilance. Sponsors and CROs rely on Saama for data aggregation and artificial intelligence solutions that lead to better decision-making, eliminate delays, and significantly shrink drug development costs and timelines. Saama can put you on the fast track to clinical trial process innovation. When all your clinical data is in one place and updated in real time, life’s much easier for your ClinOps and medical review teams. Data Managers have been underappreciated for too long. Eliminate manual work so they can pay attention to the data points that matter. -
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Florence eBinders
Florence Healthcare
Eliminate inefficient document workflows wasting time and money, limiting your ability to scale and attract new studies. Florence eBinders integrates all of your clinical trial systems, automates eRegulatory processes, reduces contract negotiation time, tracks study progress, and enables secure remote monitoring on the industry-standard eRegulatory, eISF, and eSource platform. Florence eBinders integrates all of your clinical trial systems, automates eRegulatory processes, reduces contract negotiation time, tracks study progress, and enables secure remote monitoring. Get your team and study set-up fast and all users transitioned with our top-ranked implementation and support teams. Most sites are fully up and running in four weeks! Reduce time spent in on-site monitor visits by turning on secure access to your monitors, as well as remote access capabilities for your team. -
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Clario Imaging Platform
Clario
Clario’s Imaging Platform is a secure, streamlined solution that provides you with accurate results for clinical trials of any complexity. We leverage our in-house medical expertise and our proprietary imaging systems to design your workflow and analysis to meet your unique needs. Using our dedicated engineering teams, you eliminate the extra layers of cost and time associated with relying on third-party systems. Clario is the world’s leading Imaging Core Lab with more than 30 physicians and 35 scientists dedicated to medical imaging. Our decades of experience in assessing and reviewing medical images have informed the development path of our proprietary imaging systems. Clario’s SMART Submit application incorporates this expertise every step of the way, from the second it screens a medical image for errors at the hospital, to the final image interpretation. -
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Fluency for Imaging
Jacobian
Fluency for Imaging is an AI-powered radiology reporting platform developed by Jacobian to help radiologists create accurate and efficient diagnostic reports. The platform combines advanced speech recognition, AI-assisted reporting, and seamless PACS integration to streamline the radiology reporting workflow. Fluency for Imaging enables radiologists to dictate reports naturally while the system structures the narrative into organized clinical documentation. Built-in quality controls and guideline support help ensure compliance and reduce errors during report creation. By automating routine documentation tasks and reducing cognitive workload, the platform helps radiologists focus on clinical interpretation while improving productivity and patient care outcomes. -
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MiNNOVAA
MiNNOVAA
MiNNOVAA is a medical information technology company providing solutions in the field of medical imaging software and medical image exchange. Our motto is 'medical imaging innovation,' and our key characteristic is the agility and cutting-edge technology we employ to develop our solutions. Our primary focus areas include medical image viewer, radiology workflow, and artificial intelligence in diagnostic reporting. With a young and dynamic team consisting of approximately 20 programmers and product managers, along with colleagues in marketing, sales, technical support, call center, and administration, we strive to make a significant transformation in medical imaging and contribute to individual healthcare. Our clinical imaging IT solution caters to mid-size hospitals and imaging clinics, providing an extensive range of features, including on-premise core PACS software, DICOM web viewer, imaging workstation software (multi-platform), integration with EHR/EMR/HIS, and workflow engine/RIS. -
11
WorkstationOne
Three Palm Software
Three Palm Software’s breast imaging workstation product¹ is called WorkstationOne, and offers a distinctly different style of enterprise integration and interpretation workflow. Three Palm Software understands the data-intensive challenges that radiologists are facing when moving to digital mammography, and the need to review digital mammograms as efficiently as they can read films on motorized lightboxes. This mammography workstation’s elegant and simple interface is designed to meet the most demanding radiologists’ needs. Incorporates expert viewing methodology including Tabár’s systematic viewing mask techniques* for searching for subtle radiographic abnormalities. Full-resolution image viewing navigated using a mouse wheel with visual tracing of pixels that have been viewed – no need to manually pan and zoom the images to view all pixels at full resolution. -
12
Veeva SiteVault
Veeva Systems
Streamline regulatory operations across your organization to improve compliance and advance research. Veeva SiteVault reduces the complexity of conducting clinical trials by connecting your regulatory operations to improve efficiency and compliance. Manage regulatory and source documents in a single system that supports 21 CFR Part 11 and HIPAA requirements. With a real-time visibility across trials, SiteVault Enterprise improves operational efficiency, speeds study activation, and enables faster, higher-quality trial execution. Replace manual processes and design your own workflows to support quality and speed study activation. Eliminate the need to grant EMR access or redact documents by providing monitors with secure, direct access to your regulatory and source documents. Create your own workflows, reports, and dashboards for greater visibility into start-up timelines and regulatory processes. -
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BRIT Systems
BRIT Systems
Our single cloud-based solution helps you consolidate your facility or health system’s radiology services under one contract and drive down costs without compromising the quality, reliability, or accessibility of imaging studies. BRIT Systems is a pioneer of modern imaging solutions for the healthcare enterprise. Their single cloud-based solution helps consolidate radiology services under one contract, driving down costs. The company offers a quality control module designed to enhance quality performance across radiology ecosystems, creating value for both facilities and their patients. Explore the modules contained in our cloud-based solution to see how each creates value for our partner facilities and their patients. No radiology solution is one-size-fits-all. We recognize that our full suite of services may be more than some facilities require. Once any of our services are implemented in your facility, any additional modules you may need can be made available to you. -
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PowerScribe One
Microsoft
PowerScribe One is a next-generation radiology reporting platform powered by AI, designed to improve diagnostic accuracy and workflow efficiency. Integrated with Microsoft Cloud for Healthcare, it automates several aspects of radiology reporting, including generating draft impressions and offering real-time clinical guidance. Features like Smart Impression, AI findings, and clinical decision support help radiologists produce content-rich reports faster and with fewer errors. PowerScribe One also supports seamless integration with electronic medical records (EMR) and offers cloud-based speech recognition for more accurate and efficient documentation, ultimately leading to improved patient outcomes. -
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PDQuest
Bio-Rad Laboratories
PDQuest 2-D analysis software, version 8.0, offers comprehensive and flexible 2-D gel electrophoretic analysis. Choose PDQuest Basic for simple 2-D gel analysis or PDQuest Advanced for the latest available features for 2-D gel-based expression proteomics studies. Whether you choose the basic or advanced version, the sophisticated analysis tools reveal subtle differences among 2-D gels. Powerful auto-matching algorithms quickly and accurately match gels with little or no manual intervention. PDQuest software's flexible annotation features make it a useful tool to establish a centralized information repository, which allows virtually any type of characterizing data to be linked to each spot on a master gel image. It is easy to view and share information associated with identified proteins. Spot cutting configurations for high accuracy, high throughput, and flexibility in protein identification experiments. -
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Ambra Health
Ambra Health
Ambra Health is a sophisticated cloud-based medical data and image management platform for hospitals, radiology practices, medical groups, and contract research organizations. Scalable, intuitive, and highly interoperable, the Ambra Health software empowers healthcare providers to improve collaboration by allowing efficient image exchange with their patients and departments. Ambra’s secure storage solution enables users to save all imaging within a single repository and allows them to store various types of medical imaging file formats including TFF, JPEG, DOC, and more. Core features include EMR HL7 Bridge, PACS integration, Cloud VNA, EMR / EHR integration, telestroke, informatics-first migration, and more. -
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Quantib Brain
Quantib
Quantib Brain is an FDA-cleared and CE-marked radiology software solution for brain scan segmentation. Developed in collaboration with GE Healthcare, it functions as a plug-in for the Advantage Workstation (Server), offering automated brain structure quantification within a familiar software environment. The software enables longitudinal comparison of quantified brain volumes, including white matter, grey matter, intracranial volume, and cerebrospinal fluid, facilitating the tracking of atrophy development. Additionally, it provides the option for white matter hyperintensity segmentation and monitoring. Quantib Brain presents a clear overview of volumes for grey matter, white matter, ICV, CSF, and total brain volume in an informative results table. These results, supported by self-selected cross-sections, can be exported into a comprehensive report. The software ensures that all examination results can be shared instantly. -
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Q/ris 3000 Workflow
medQ
Intelligent, intuitive, and rules-driven online scheduling and room management to simplify patient booking, making it fast and virtually error-free. Automatic scheduling of complex segmented procedures. Efficient and paperless patient registration and document management. Upfront, online real-time insurance verification. Manage any number of facilities at once. Integrated auto CDS tool. In addition to automatically capturing DICOM SR data, the Q/ris technologist workflow module is packed full of tools to help your technologist prepare more data-rich studies while saving time for your radiologist. Automatic generation of exam-specific electronic worksheets for technologist notes and annotations. Real-time editing, modifying or rescheduling of exams at any point. Automatic charge capture and interactive supply capture. MIPPS compatible DICOM modality worklist. Automatically capture DICOM SR data from the modality. -
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FICS
Pi Health
Accelerating the development of lifesaving medicines and enabling patients globally to have equal access to the highest quality of cancer care and research. Our software is revolutionizing patient access to innovative medicines & clinical trials. FICS is an innovative software that enables the collection of regulatory standard data during patient care. FICS brings together traditionally separate and non-communicating applications into a novel, end-to-end platform, paving the way for clinical trials to be done easier, faster, and with great quality. -
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AIATELLA
AIATELLA
Every year, cardiovascular diseases claim over 20 million lives worldwide. Many of these deaths could be prevented with early detection. Yet, the global healthcare system is overwhelmed, and limited by human capacity for detailed analysis. That's where AIATELLA steps in. Our groundbreaking AI-powered image analysis solution transforms the landscape of cardiovascular diagnostics. By automating manual measurements of vasculature in a quantified way and using historical data, we drastically cut down on the time, cost, and level of expertise needed, significantly expanding the capacity for critical imaging. AIATELLA's solution improves the speed, accuracy, and precision of diagnostics, delivering measurements and disease-progression analysis in seconds instead of hours. By improving the speed, accuracy, and variability in the analysis we are enabling the doctors to spend more time with patients and enabling true preventative and personalized medicine for all. -
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DatCard
DatCard Systems
Hospitals and imaging centers are inundated with discs from outside organizations. The manual importation of data is not only very time consuming, but also very costly. With Automated Disc Importer, organizations have the added ability of importing volumes of discs into temporary cloud-based or local storage through an automated process, eliminating the need for human intervention. Once discs are read, users may reconcile the data and import into their archive. As an added security benefit, the Automated Disc Importer takes a photograph of every disc label that is being read for purposes of audit trail reporting. The photograph clearly identifies where the disc was created. The Automated Disc Importer ingests medical images and reports from DICOM discs, drastically reducing time spent on manual importing. -
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Elucis
Realize Medical
Realize Medical's Elucis is an FDA-cleared extended reality platform that enables users to easily segment images, collaborate with multiple remote colleagues, and plan procedures within a virtual reality environment. Elucis supports unlimited import of 3D and 4D CT and MR images, allowing for comprehensive project integration. The platform offers advanced image processing capabilities, including manual and automatic image registration, as well as 2D, 3D, and 4D image display. Its segmentation tools are designed for speed and ease of use, facilitating measurement, cutting, and planning directly in virtual reality. Elucis also features sophisticated 4D modeling tools, enabling detailed segmentation of cardiac structures across all phases in minutes. Users can import 3D structure files from other sources and export their creations with a single click. The platform supports multi-user collaboration, allowing connection with local or remote colleagues at any point in the workflow. -
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Unlearn
Unlearn
Advancing AI to eliminate trial and error in medicine. Our digital twins enable confident and quick clinical trials. We work in neuroscience, immunology, metabolic disease, and more. TwinRCTs reach full enrollment sooner because they require fewer patients to achieve the same power as traditional trial designs. Shorten time to enrollment in late-stage studies. TwinRCTs improve the ability to observe treatment effects in early-stage studies by increasing power without adding more patients. Make confident decisions from early-stage studies and attract study participants. TwinRCTs give participants a greater chance of receiving the experimental treatment because they use smaller control groups. Position clinical trials with digital twins for regulatory success. Unlearn is engineering the future of medicine with artificial intelligence. We invent and deploy new types of generative models trained on extensive patient-level data from previous studies. -
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ClearRead Xray
Riverain Technologies
Riverain Technologies' ClearRead Xray is a suite of five FDA-cleared applications designed to enhance the efficiency and accuracy of chest X-ray interpretation across healthcare enterprises without necessitating additional equipment, procedures, or radiation exposure. The platform employs unique suppression technology to provide an unobstructed view of the chest, facilitating the rapid and accurate detection of cardiothoracic diseases. Key features include the production of bone-suppressed images for improved visualization, identification of potential lung cancer nodules, reduction in portable X-ray reading time, automatic comparison of findings with prior exams to highlight changes, and enterprise-wide compatibility across various manufacturers and imaging protocols. Notably, ClearRead Xray Bone Suppress increases the visibility of soft tissue by suppressing bone structures in digital images, aiding radiologists in detecting previously missed nodules. -
25
Clindata Cloud
Clinical Data
Clindata Cloud receives pre-clinical / clinical / Risk Metric data from multiple data sources/sites, and empowers the clinical operations teams, with submission-ready data sets, analytics and risk-based monitoring alerts. Consolidate & harmonize study data from multiple data sources into a comprehensive study data model. Validate received data for completeness, accuracy, integrity and consistency and raise alerts and notifications in case of exceptions or risk patterns. Standardize data to CDISC data standards, to eliminate noise and create submission-ready data sets in real-time for continuous validation of data & analysis. Generate submission-ready analytics in real-time based on standardized data. -
26
RADIOLens
Synapsica
Radiolens is an AI-enabled PACS radiology workflow solution that makes diagnostic workflows smoother by automatically detecting bad-quality scans and creating preliminary reports for some most common modalities. It enables clinical collaboration, provides workflow efficiency, and enables well-informed decision-making. Automated assignments for workload optimization. Get AI-enabled quantitative and qualitative actionable insights to boost your reporting speed and accuracy. Lightweight DICOM Viewer to open cases even from mobile devices. Remove on-site presence constraints with an on-cloud solution. Get real-time notifications on your device! Best accuracy, Unlimited backup, and Simple archiving of images. Get instant AI-assessed biomarkers for qualitative and quantitative descriptions such as CCAP diameter, listhesis, compression fractures, IV disc height, and thecal sac. Our intelligent server auto-matches templates to studies based on patient gender and modality. -
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REDCap Cloud
REDCap Cloud
REDCap Cloud is a unified data-science platform that enables organizations to collect, integrate, standardize, analyze, and share real-world and regulatory-grade clinical and research data using a single standards-based system. It supports the full lifecycle of randomized clinical trials and real-world evidence studies by offering modules for complex trial design and deployment, a clinical data hub that converges eCRF and non-eCRF sources, real-time operational and data insights via AI/ML, eSource and EHR connectivity, patient engagement (ePRO/eCOA, wearable devices) for hybrid or decentralized trials, analytics including synthetic control arms and digital twins, and global compliance with security standards, all built to reduce data-silos, eliminate vendor fragmentation, deliver bidirectional data flows and give sponsors, CROs and health-systems end-to-end visibility and control across site performance, study data quality and regulatory readiness. -
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Cloudbyz CTMS
Cloudbyz
Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. Cloudbyz provides end-to-end management of the clinical trial lifecycle, including study setup, site management, study projections, monitoring, and financial management. With Cloudbyz, you can optimize your study planning, accelerate patient recruitment, and increase trial quality, while reducing costs and minimizing risk. -
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TrialKit
Crucial Data Solutions
TrialKit is a unified eClinical platform designed to support the full lifecycle of clinical trials, from study design through data analysis. Built for sponsors, CROs, and research sites, TrialKit combines EDC, ePRO/eCOA, eConsent, RTSM, medical coding, imaging, and more in a single configurable system. Its drag-and-drop study builder enables rapid setup of compliant studies without programming, while web and native mobile apps support secure, real-time data capture from any location. TrialKit AI extends the platform with advanced analytics, study simulation, and protocol validation, helping teams evaluate design decisions and identify risks earlier. With API-based integrations and support for global compliance standards, TrialKit reduces system fragmentation, improves efficiency, and provides a scalable foundation for modern clinical research. -
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ORS Dragonfly
Object Research Systems
Powerful, flexible, and user-friendly, Dragonfly delivers quantitative answers for today's most demanding 2D/3D/4D imaging studies, including data from correlative and hyperspectral imaging systems, X-ray, SEM, FIB-SEM, ion beam, and confocal microscopy, as well as other advanced applications. Gain detailed insight into material structures and properties with interactive inspection tools and robust quantification workflows. Post-processing functions include data restructuring, filtering, volume and slice registration, image stitching. Powerful segmentation tools to accurately label image features. Meet image enhancement and segmentation challenges with Dragonfly's Deep Learning solutions. Automate your 3D analysis workflows with easy-to-author macros. Dragonfly with Deep Learning is a transformative solution for image processing. Experience the only commercially-supported Deep Learning engine that lets you train and execute custom networks. -
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EvidentIQ
EvidentIQ
eCOA by EvidentIQ optimizes real-time, direct-from-patient data collection by offering a simple and intuitive interface providing advanced patient assessments to enhance the patient experience and improve data quality. Customers can benefit from an end-to-end comprehensive eCOA package or create value by selecting from the various elements meeting specific requirements. Book a demo with our team of experts and see how you can improve your study ROI. eCOA by EvidentIQ brings data science services and technology together. Customers can benefit from an end-to-end comprehensive eCOA package or create value by selecting various elements meeting specific requirements. The solution can be used stand-alone as it is independent of any specific eClinical technologies such as EDC systems, but it can be integrated in any existing eClinical software landscape. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way. -
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Rave CTMS
Dassault Systèmes
Study teams are increasingly being challenged to do more with fewer resources. Delays caused by disconnected systems, manual data re-entry, redundant workflows, and information silos can seriously affect a trial’s progress. You need a clinical trial management system that unifies and streamlines workflows while still maintaining full visibility, and Medidata has the solution. Rave CTMS is the only data-driven solution for faster, smarter, end-to-end trial management. As an integral part of the Medidata Rave Clinical CloudTM, Medidata provides all of the elements you expect from an industry-leading CTMS and more. Rave CTMS provides your study teams with the ability to plan and manage all of your clinical trials in a consistent and harmonized manner that standardizes activity planning and management at the study, country, and site level. Activities include study/site team creation and activation, patient enrollment and milestone tracking, site monitoring, and issue management. -
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Zelta
Merative
Zelta is a cloud-based unified clinical data management and acquisition platform with adaptable modules that can be tailored to meet the unique needs of your clinical trials program and accelerate outcomes. It offers features such as electronic data capture, clinical operations tools like randomization and trial supply management, clinical trial management system, electronic trial master file, and patient and provider engagement solutions including electronic clinical outcome assessments and electronic consent. Zelta is designed to manage clinical studies across all phases, therapeutic areas, and regions, providing a user-friendly interface and seamless access through single sign-on from anywhere in the world. The platform emphasizes flexibility and scalability, allowing for customization to align with specific study goals and the integration of solutions from both Zelta and other technology vendors. -
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uMotif
uMotif
uMotif is a modern eCOA/ePRO and eConsent platform designed to power clinical and real-world research. Developed in collaboration with patients, the platform delivers unrivaled engagement, transforming the speed, quality, and accuracy of data. By combining uMotif's eCOA/ePRO with continuous glucose monitoring data capture, the platform delivered unprecedented data compliance rates for a pan-European diabetes study. In an immunology study, the patient-centered eCOA/ePRO solution helped the sponsor complete data capture requirements six months early. In an FDA-required CNS study, participants were engaged to capture submission-ready ePRO through their own devices. uMotif has always designed for patients first, with a relentless focus on understanding the patient journey and what drives patient behavior. This deep knowledge allows the design of software that best meets the needs of patients and delivers exceptionally high levels of engagement to study sponsors. -
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NeuroQ
Syntermed
NeuroQ is a leading brain imaging analysis software that provides a powerful diagnostic tool available for multiple modalities and clinical applications. It offers an integrated solution for FDG, Amyloid, SPECT, DaTscan, and Epilepsy, supporting the most relevant functional imaging modalities to increase accuracy in differential diagnosis. NeuroQ is one of the most widely used quantitative tools for the differential diagnosis of dementia. The software goes beyond visual reads by providing valuable non-subjective diagnostic information, rapidly comparing metabolic levels in more than 240 predefined regions of the brain to a normal database, and quantifying the degree of abnormality and statistical significance of the findings. NeuroQ has been developed to aid in the assessment of human brain scans through quantification of mean pixel values lying within standardized regions of interest, and to provide quantified comparisons with brain scans. -
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Popsipen
POPSICUBE
Popsipen is a unique Digital Pen and Paper Technology. It captures the handwriting and transfers it to a database via a USB or Bluetooth connection. As easy to use as a regular pen, this device is a very user friendly way of transferring secured data in real time, on a global scale. We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications specific to the pharmaceutical industry. Our flexibility and experience in the pharmaceutical market, while always maintaining a cost-conscious approach, differentiates us from other CROs. We are able to respond to the changing requirements of the study without time-consuming CRO bureaucracy and delayed deliverables. We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications.Starting Price: $1000.00/one-time/user -
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Cenduit IRT
Cenduit
Today’s Interactive Response Technology (IRT) systems are increasingly complex. Flexible and configurable IRT matters - with IRT data as the source of record for recruitment, clinical trial drop-out rates, patient visits, and other crucial data. Choose a platform that’s user-friendly, mobile-ready, and comprehensive - embedded in quality, flexibility and expertise. Choose comfort with complex therapeutic expertise in today’s risk-based eClinical environment. Combining the right technology, subject matter expertise and commitment to service we empower clinical trials to deliver patient outcomes. Deep clinical and supply chain knowledge drives innovation and provides clients with control over their Randomization and Trial Supply Management (RTSM) processes. Our innovative suite of tools drives distinctive levels of quality control, site efficiency and patient compliance. Our IRT platform can meet the needs of almost any study, enabling fully validated deployment in as little as 30 days. -
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Ripple Science
Ripple Science
Ripple is a web-based software solution and active registry that facilitates the recruitment and management of research participants for clinical, translational and social science studies. Built from the ground up by researchers for researchers to truly transform participant workflow, Ripple is an end-to-end research participant management software that accelerates the entire research life cycle. Applying technology to solve patient recruitment and retention challenges, the #1 reason cited when clinical trials fail. The success of clinical trials and translational studies greatly depends on the ability of research teams to meet enrollment targets on time and on budget. Ripple Recruit empowers research teams with the automation tools and analytics necessary to accelerate the recruitment processes and maximize the likelihood of study success. Ripple Recruit provides critical insights into your recruitment campaign and workflows, including what sources are most effective. -
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Silverback
DataFirst
Increase efficiency and empower your team to make intelligent decisions that impact IT operations and patient outcomes. Seamless integrations and the highest data security standards empower data access from any location, viewer, device, exchange, or portal. Eliminate legacy migration tools and multiple vendors to unlock cost savings and efficiency gains of a system-wide, unified imaging network. Silverback gets smarter, stronger, and faster with every data interaction. Over time, the engine identifies and tracks patterns to deliver predictive insights throughout the image network. As the foundation of the Silverback platform, Vue is a dynamic DICOM router that intelligently distributes studies throughout the enterprise. The router orchestrates images for multiple sites and multiple vendors through customized logic rules. Vue may be placed in front of the PACS or behind the modalities to best capture, manage, and distribute studies throughout the network. -
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Omda MedSciNet
Omda
Omda MedSciNet solutions improve the quality, utility, and management of medical data from collection to analysis. This secure standardized software makes it easy for clinical researchers and other professionals in medicine and academia to gather and analyze well-managed medical data. The Omda team specializes in building and managing tailor-made database applications and designing clinical studies for medical research and quality registers. The Omda MedSciNet study platform provides a reliable, feature-rich, and highly customizable online environment for hosting and managing sophisticated study and clinical trial systems. Omda MedSciNet has a 20-year track record of successfully hosting studies and clinical trials of all scopes and sizes. The standard implementation includes a comprehensive set of components necessary for establishing fully functional studies or clinical trials. -
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Clinical Ink
Clinical Ink
Get on the path to cleaner data and confident decisions with Clinical Ink. As the pioneers in eSource, Clinical Ink’s technology platform and delivery capabilities provide greater certainty from source to submission. Explore Lunexis™, a clear and connected eSource Ecosystem that delivers purpose-built data capture solutions for your protocol at the critical moments that matter. The Lunexis platform makes it easy to deploy an integrated, convenient eSource solution that provides anytime, anywhere access to your study data. We deliver more than fast, clean data — we deliver confidence. Not only are your sites and patients assured of an easier experience, but you can be certain that your patients are more compliant and engaged and that your protocol is executed correctly. Start your most complex studies with confidence — implement Lunexis to support well-informed, optimal decisions. -
42
MIStar
Apollo Medical Imaging Technology
Apollo Medical Imaging Technology is a clinically-driven medical imaging software company specializing in the creation of advanced image processing software for clinical and research applications. Their flagship product, MIStar, is a fast, economical, and easy-to-use software package that provides a broad spectrum of advanced functions and cost-effective cross-modality solutions for clinicians and the OEMs that serve them. MIStar supports various imaging modalities, including CT, MR, NM, and PET, and offers advanced modules such as CT Perfusion for stroke, brain tumor, body tumor, liver, kidney, and prostate; DSC-MRI for stroke; DCE-MRI for brain tumor, breast, body tumor, liver, kidney, and prostate; DWI & ADC; DTI Fiber Tractography; NM Renogram Analysis; and Image Fusion. The software features data access and image input through DICOM networking functions, an intuitive clinical database, and easy anonymization and archiving. -
43
Oracle Clinical One
Oracle
Clinical One RTSM can support a randomization strategy for the simplest to the most complex studies without the need for programming or coding, which eliminates the need for prolonged user acceptance testing. Take control of your study through self-service configurations and build a study in days instead of weeks. Assess the status of the drug inventory and make modifications in real-time without reverting to the vendor and incurring cost and change requests. Eliminate change request costs and avoid delays by quickly implementing changes and promoting your studies in seconds. The only platform that truly unifies people, processes, and data to simplify and accelerate the clinical trials of the future. Virtual components in clinical trials allow greater patient participation and significantly improve clinical trial data quality. Transformative digital strategies are needed for faster study startup to harmonize data from any source and to streamline workflow. -
44
eDeviation
eDeviation
eDeviation supports all the operations for Protocol Deviation assessment and management. From software design and validation to collecting supporting documents and exporting data for the TMF, eDeviation® relieves your clinical team from the risks associated with missing or wrongly assessing one-time or recurring protocol deviations. eDeviation® is part of Ethical’s eClinical Software Platforms Solutions supporting faster and more accurate clinical trials management. Whether your protocol deviation assessments are performed by an independent expert committee or by your study team, our eDeviation® software is configured to exactly match your needs. Forms, workflows and exports altogether contribute to a GxP quality and effectively managed study. Study teams, Investigators’ Sites and Committee Members, when applicable, work seamlessly online in real-time to expedite judgments, consensus and timely completion of the protocol deviation assessments and management. -
45
Novatek Clinical Assay Management Software
Novatek International
Novatek’s Clinical Assay Management software is a unique information management application that provides a consistent approach to the collection, management and integrity of clinical research study data. Novatek’s Clinical Assay Management software tracks and manages all sample data throughout its whole analytical process and ensures a single verifiable version for all clinical and analytical data sets. Novatek’s Clinical Assay Management software `helps organizations manage their studies based on a particular product that is being developed. In addition, this application will give clinical studies the structure that is required to ensure all related steps are executed in a timely manner. -
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cubeCTMS
CRScube
cubeCTMS is a comprehensive clinical-trial management system designed to provide end-to-end oversight of trials, from site and investigator tracking, enrollment management and visit scheduling through budget and contract workflows, milestone reporting and document control. It centralizes study operations and automates key processes so sponsors, CROs and study teams can monitor progress in real time, manage tasks across multiple studies, improve site communications and mitigate risk. With built-in dashboards, alerts and audit-ready logging, cubeCTMS supports regulatory compliance (including FDA 21 CFR Part 11 readiness) and enables stakeholders to manage trial timelines, resources and performance from one platform. The system integrates with other CRScube modules (such as EDC, eTMF, pharmacy/RTSM) to provide a unified ecosystem that reduces duplication, improves data flow and supports adaptive workflows during amendments or global roll-outs. -
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PACScribe
Folio3 Digital Health
PACScribe is a cloud-based PACS imaging software designed to help clinicians and healthcare providers manage and analyze medical imaging data more efficiently. The platform provides secure access to DICOM tools that allow users to view, share, and collaborate on medical images in real time. PACScribe supports multiple imaging modalities such as MRI, CT scans, X-rays, ultrasounds, and other specialized imaging studies. The system includes AI-powered report generation that analyzes imaging data and produces structured reports to assist clinicians with faster diagnosis. A built-in DICOM viewer and secure sharing tools enable healthcare teams to collaborate easily and review scans from different locations. PACScribe integrates with electronic health record systems such as Epic to centralize patient information and streamline clinical workflows. With scalable cloud storage and strong compliance standards like HIPAA and GDPR, PACScribe ensures secure and reliable medical image management.Starting Price: $119/month -
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MAISi
Agile Health Computing
Until now, the options available for managing clinical trials at an investigator site were either keeping multiple shared spreadsheets or buying expensive software unsuited to Australian conditions. MAISi is the game-changer. Beginning as a repository for clinical trials data at a major hospital in 2001, MAISi has evolved into a sophisticated workflow application to assist in most aspects of a research unit’s operations. MAISi acts as a central repository of data to store information about studies and the business units that run them. The datasets are arranged to support management decision-making. Staff in each business unit have access to the data (Studies, Patients, Investigators, Study Team Members) associated with their own business unit, whereas staff granted global access (normally Financial Officers and System Administrators) have access to all data. -
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ClinAccess
MAJARO InfoSystems
ClinAccess™ 5.1 is the next generation of our industry leading Clinical Data Management System based entirely on SAS® 9. It leads the way in simplifying clinical data management, clinical trial analysis and preparation of electronic submissions. Having your data keyed directly into SAS® data sets enhances your staff’s productivity by eliminating the time spent transfering data from Oracle/SQL into SAS. ClinAccess™ is designed expressly for ease-of-use study definition, data entry and management with features to monitor the progress and quality of ongoing clinical trials. Whether for review, analysis, or FDA submission, your data is always in SAS®and ready for analysis. The database structure is designed to support and accelerate statistical analysis and reporting. The result is less time and effort for data analysis and a shorter time to market. For reliability, auditing and security, there is no better solution than ClinAccess™. -
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Clindex
Fortress Medical Systems
A Clinical Data Management System (CDMS), Clinical Trial Management System (CTMS) and Electronic Data Capture System (EDC) all in one powerful, integrated solution. All your study information can be at your fingertips with our innovative, flexible and compliant Clinical Trial Software System. Our servers or yours. Clindex® can be installed on your servers or it is available on the Fortress Medical Cloud (SaaS – Software as a Service). Cloud access is available world-wide and your data is securely stored at a SOC 3 certified data center. You can build, we can build. Clindex® provides all the tools you need to develop your own study database. Our quick start manuals and help documentation walk you through the process, step by step. Or our Clindex services team can develop a study for you.