Alternatives to QMENTA

Improve radiology reporting efficiency and report quality with Imorgon's reporting automation. As the top DICOM SR software for radiology, our solution significantly reduces unnecessary dictation by precisely transferring ultrasound and DEXA modality measurements into Powerscribe, Fluency, or RadAI. This eliminates manual errors and significantly accelerates the generation of reports. Imorgon's unique advantages include: - guaranteed transfer of all measurements - usually DICOM SR - electronic worksheets for direct report population (eliminating dictation from notes) - worksheets with priors, calculators, and clinical decision support (TI-RADS, O-RADS, etc) - integration with Epic and other EHRs. - vendor-neutral Our dedicated support team ensures uninterrupted workflow. Invest in Imorgon for a quick and substantial return on investment, transforming your reporting overhead into a streamlined, high-quality operation.

We streamline the intricacies involved in managing your complete product lifecycle. Designed for user-friendliness and flexibility to meet your organization’s specific requirements, STARLIMS lab informatics solutions cater to the evolving demands of data management throughout your organization. Our laboratory information management systems (LIMS software) can seamlessly connect with your existing infrastructure, while also pinpointing areas for process enhancement, enabling you to accelerate the market introduction of high-quality and safe products. In doing so, we empower your organization to thrive in a competitive landscape.

ProtonPACS, a picture archiving solution, manages image storage, distribution, and optimizes workflow throughout the organization. It offers front and back-end patient management solutions that reduce manual and/or duplicate patient information entry. Integration of HL7 to information systems (EHRs, RISes, etc.) The platform includes this feature. ProtonPACS includes Intelerad's Inteleviewer. This diagnostic viewer gives radiologists and other healthcare professionals the tools to optimize images and change layouts, measure critical points, perform image reconstructions, and create key images. Radiologists can use the integrated speech recognition engine and worklist to create reports for referring doctors. Both reports and images are accessible via any web-enabled device from the system's portal. ProtonPACS uses a secure hybrid model that combines on-premise hardware and cloud hosting.

Three Palm Software has developed a breast imaging workstation named WorkstationOne, which features a unique approach to enterprise integration and interpretation workflow. Recognizing the challenges faced by radiologists transitioning to digital mammography, the company emphasizes the importance of enabling efficient reviews of digital mammograms that match the speed of traditional film readings on motorized lightboxes. The workstation boasts a sleek and user-friendly interface tailored to accommodate the rigorous demands of radiologists. It employs advanced viewing strategies, such as Tabár’s systematic viewing mask techniques, to enhance the detection of subtle radiographic abnormalities. Users can navigate full-resolution images seamlessly with a mouse wheel, allowing for visual tracking of pixels that have already been examined, thus eliminating the need for manual panning and zooming to ensure all pixels are viewed in their highest clarity. This innovation not only streamlines the workflow but also enhances diagnostic accuracy for healthcare professionals.

Flywheel provides comprehensive data management solutions to researchers looking to improve productivity and collaboration in imaging research and clinical trials, multi-center studies, and machine learning. Flywheel provides end-to-end solutions that streamline data ingestion and curate it to common standards. We also automate processing and machine-learning pipelines. Our platform allows for secure collaboration in the life sciences, clinical, academic, as well as AI, industries. Cross-platform data and algorithm integration, secure and compliant data discovery among a global network, and cloud-scalable and on-premise computational workflows to support research and clinical applications. Flywheel is a data curation platform that supports multi-modality research. It can manage a wide range of data types, including digital pathology, imaging files, clinical EMR data and omics, as well as instruments.

Clario’s Imaging Platform offers a secure and efficient solution that ensures precise results for clinical trials of varying complexities. We utilize our in-house medical specialists and proprietary imaging technologies to tailor your workflow and analysis according to your specific requirements. By employing our dedicated engineering teams, you can avoid the additional costs and time delays commonly associated with third-party systems. As the leading Imaging Core Lab globally, Clario boasts a team of over 30 physicians and 35 scientists who specialize in medical imaging. Our extensive experience in evaluating and analyzing medical images has significantly shaped the evolution of our proprietary imaging solutions. The SMART Submit application from Clario integrates this wealth of expertise at every stage, beginning with the initial screening of medical images for errors at the hospital and continuing through to the final interpretation of the images. In doing so, we ensure that every aspect of the imaging process meets the highest standards of quality and accuracy.

Solventum Fluency for Imaging is an innovative AI-driven solution designed for radiology reporting that seamlessly integrates advanced speech recognition capabilities with immediate clinical insights, efficient workflow management, and tools aimed at boosting productivity to enhance quality, compliance, efficiency, and cost-effectiveness. This software maintains existing workflows while transforming dictations into precise, high-quality documents that are well-structured, clinically encoded, easily searchable, and readily shareable. It employs natural language understanding to accurately interpret the context of radiologists' dictations and includes built-in computer-assisted physician documentation, offering automated and interactive clinical insights directly within the reporting process. Additionally, the solution features customizable templates, personalized macros, and workflow enhancements such as actionable findings management and peer reviews, all aimed at ensuring thorough capture, documentation, and communication of patient outcomes. By integrating these functionalities, Solventum Fluency for Imaging significantly improves the overall efficiency of the radiology reporting process.

Cardiovascular diseases result in more than 20 million fatalities globally each year, many of which could be avoided through timely detection. Unfortunately, the healthcare sector is often stretched thin, hindered by the limitations of human analysis capabilities. This is where AIATELLA makes a significant impact. Our innovative AI-driven image analysis technology revolutionizes cardiovascular diagnostics. By automating the intricate measurements of blood vessels and leveraging historical data, we substantially reduce the time, expenses, and required expertise, thereby enhancing the potential for vital imaging procedures. AIATELLA's approach not only accelerates the diagnostic process but also boosts the precision and reliability of results, providing critical measurements and disease progression insights in mere seconds rather than hours. As a result of this increased efficiency and accuracy in analyses, healthcare providers can dedicate more time to patient care, ultimately paving the way for effective preventative strategies and personalized treatment options for everyone. This shift could redefine how we approach cardiovascular health on a global scale.

Version 8.0 of PDQuest 2-D analysis software provides a robust and adaptable platform for conducting 2-D gel electrophoresis analysis. Users can opt for PDQuest Basic for straightforward 2-D gel evaluations or PDQuest Advanced to access the most cutting-edge features designed for in-depth expression proteomics research. Regardless of the version selected, the advanced analytical tools effectively highlight subtle variations across different 2-D gels. The software employs powerful auto-matching algorithms that ensure quick and precise gel matching with minimal manual effort. Furthermore, PDQuest's versatile annotation capabilities make it an invaluable asset for creating a centralized database, enabling a wide array of characterization data to be associated with each spot on a master gel image. Sharing and reviewing information related to identified proteins is made simple and efficient. Additionally, the software offers adaptable spot cutting configurations that enhance accuracy, throughput, and flexibility in protein identification trials, making it an essential tool for researchers in the field.

MiNNOVAA is a company specializing in medical information technology, particularly in the realms of medical imaging software and the exchange of medical images. With the guiding principle of "medical imaging innovation," we stand out for our nimbleness and the state-of-the-art technology we utilize in crafting our solutions. Our main areas of concentration are the development of medical image viewers, enhancement of radiology workflows, and the incorporation of artificial intelligence in diagnostic reporting. Our energetic team comprises around 20 skilled programmers and product managers, alongside professionals in marketing, sales, technical support, call center operations, and administration, all dedicated to driving a meaningful transformation in the field of medical imaging and enhancing individual healthcare experiences. We offer a comprehensive clinical imaging IT solution tailored for mid-sized hospitals and imaging clinics, featuring a wide array of functionalities such as on-premise core PACS software, a DICOM web viewer, multi-platform imaging workstation software, seamless integration with EHR/EMR/HIS systems, and an efficient workflow engine/RIS. Ultimately, our commitment to innovation and comprehensive solutions aims to redefine how medical imaging is approached and utilized within healthcare settings.

Harnessing actionable insights from the leading AI-driven clinical analytics platform allows your teams to effectively manage risk and enhance performance throughout studies, systems, sites, and vendor relationships. The cutting-edge technology from Saama is specifically crafted to optimize workflows, automate labor-intensive tasks, and foster improved collaboration among various clinical functions such as operations, medical review, data management, biostatistics, and pharmacovigilance. Both sponsors and CROs depend on Saama's capabilities for data aggregation and AI solutions, which facilitate superior decision-making, minimize delays, and drastically reduce costs and timelines associated with drug development. By leveraging Saama's tools, you can accelerate the pace of clinical trial innovation. When your clinical data is centralized and continuously updated, it simplifies the lives of your ClinOps and medical review teams considerably. Furthermore, Data Managers, often undervalued, can shift their focus from repetitive tasks to the critical data points that truly drive project success, ensuring that their expertise is fully utilized in the process. This transformation not only enhances efficiency but also contributes to the overall quality of clinical outcomes.

Our comprehensive cloud-based platform enables you to streamline your facility or health system’s radiology services under a single contract, effectively reducing expenses while maintaining the quality, dependability, and accessibility of imaging studies. BRIT Systems stands at the forefront of innovative imaging solutions tailored for the healthcare sector. This unified cloud solution not only consolidates radiology services under one agreement but also significantly cuts costs. Additionally, the company provides a quality control module aimed at improving performance across various radiology ecosystems, thereby delivering added value for both healthcare facilities and their patients. By delving into the various modules within our cloud-based solution, you can assess how each contributes to enhancing value for our partner facilities and the patients they serve. It's important to note that no radiology solution fits all scenarios perfectly. We understand that our extensive range of services might exceed the needs of some facilities. Therefore, once any of our services are integrated into your facility, you can easily access additional modules as necessary to meet your specific requirements. This flexible approach ensures that every facility can tailor their radiology offerings to best serve their unique circumstances.

An intelligent and intuitive online scheduling and room management system designed to streamline patient bookings, ensuring a swift and nearly flawless experience. It features automatic scheduling for intricate segmented procedures, facilitating efficient and entirely digital patient registration along with document management. The system offers real-time insurance verification online, allowing for the management of multiple facilities simultaneously. It includes an integrated auto Clinical Decision Support (CDS) tool, enhancing workflow efficiency. The Q/ris technologist workflow module not only captures DICOM Structured Reports (SR) automatically but is also equipped with various tools that assist technologists in producing data-rich studies, ultimately saving valuable time for radiologists. Furthermore, it automatically generates exam-specific electronic worksheets for technologist notes and annotations, allowing for real-time editing, altering, or rescheduling of exams. The system also features automatic charge capture and interactive supply capture, while being compatible with MIPPS DICOM modality worklists, allowing for seamless data integration. This comprehensive approach ensures that all processes are streamlined for optimal performance.

Hospitals and imaging facilities are overwhelmed by the influx of discs from various external sources. The process of manually importing this data proves to be both labor-intensive and expensive. However, with the implementation of the Automated Disc Importer, these organizations can efficiently transfer large quantities of discs into either temporary cloud storage or local systems without requiring human assistance. After the discs are processed, users are able to validate the data before it is officially archived. Additionally, this system enhances security by capturing an image of each disc label during the reading process, which aids in maintaining a comprehensive audit trail. These photographs not only document the imports but also specify the origin of each disc. By leveraging the Automated Disc Importer, medical images and reports from DICOM discs are effectively processed, significantly minimizing the time previously dedicated to manual data entry, and improving overall workflow efficiency. This innovation represents a substantial advancement in the management of medical imaging data.

Ambra Health offers an advanced cloud-based platform designed for the management of medical data and images, catering to hospitals, radiology practices, medical groups, and contract research organizations. This platform is scalable, user-friendly, and highly compatible with other systems, enabling healthcare providers to enhance collaboration through seamless image sharing with patients and various departments. With Ambra’s secure storage solution, users can consolidate all imaging data into a unified repository, accommodating a wide range of medical imaging file formats such as TFF, JPEG, and DOC among others. Key functionalities of the platform include an EMR HL7 Bridge, integration with PACS, a Cloud VNA, EMR/EHR integration, telestroke services, and an informatics-first migration approach. Ambra Health not only streamlines the management of medical images but also ensures compliance with industry standards, thereby promoting better patient care and operational efficiency. These features make it a crucial tool for organizations aiming to optimize their imaging workflows in a rapidly evolving healthcare landscape.

Enhance the efficiency of regulatory operations within your organization to bolster compliance and facilitate research advancements. Veeva SiteVault simplifies the process of managing clinical trials by integrating your regulatory tasks, leading to improved effectiveness and adherence to regulations. You can oversee regulatory and source documents through a unified platform that complies with 21 CFR Part 11 and HIPAA standards. With real-time insights across all trials, SiteVault Enterprise boosts operational effectiveness, accelerates study initiation, and fosters swift, high-quality trial management. Transition away from manual workflows and customize your own processes to enhance both quality and speed in study activation. By granting monitors secure, direct access to your regulatory and source documents, you eliminate the hassles of EMR access and document redaction. Furthermore, you can tailor your workflows, generate reports, and create dashboards to gain deeper insights into start-up timelines and regulatory workflows, ultimately driving better outcomes for your clinical trials. This comprehensive approach not only streamlines processes but also enhances collaboration across teams.

Streamline your document workflows to eliminate inefficiencies that consume valuable time and resources, hindering your growth and ability to secure new studies. Florence eBinders seamlessly connects all your clinical trial systems, automates eRegulatory tasks, shortens contract negotiation duration, monitors study advancement, and facilitates secure remote oversight on a leading eRegulatory, eISF, and eSource platform. With our highly-rated implementation and support teams, your team and study can be set up quickly, ensuring a smooth transition for all users. Most sites become fully operational within just four weeks! By enabling secure access for your monitors and providing remote capabilities for your team, you can significantly decrease the time spent on-site during monitoring visits. Additionally, this approach fosters a more efficient and flexible research environment.

Dragonfly is a robust, adaptable, and easy-to-use software that provides quantitative solutions for a wide range of imaging studies, such as 2D, 3D, and 4D analyses, effectively handling data from various imaging systems like correlative and hyperspectral imaging, X-ray, SEM, FIB-SEM, ion beam, and confocal microscopy, along with other sophisticated applications. With its interactive inspection tools and comprehensive quantification workflows, users can achieve in-depth understanding of material structures and properties. The software offers a suite of post-processing capabilities, including data restructuring, filtering, volume and slice registration, and image stitching. Additionally, it features powerful segmentation tools that enable precise labeling of image characteristics. Dragonfly also addresses image enhancement and segmentation challenges with its advanced Deep Learning solutions. Users are empowered to streamline their 3D analysis processes through easily created macros. By integrating Deep Learning into its functionalities, Dragonfly transforms the landscape of image processing, providing access to the only commercially-supported Deep Learning engine that allows for the training and execution of custom networks, which significantly enhances the overall user experience. This innovative approach ensures that both novice and experienced users can tackle complex imaging tasks with confidence and efficiency.

Sapio Sciences delivers a cutting-edge AI-driven lab informatics platform that integrates Laboratory Information Management Systems (LIMS), Electronic Lab Notebooks (ELN), and a Scientific Data Cloud into one seamless ecosystem. It is tailored to advance scientific research, clinical diagnostics, drug discovery, and manufacturing through configurable, no-code solutions. The Sapio LIMS® automates complex workflows with full configurability, removing the need for programming. Sapio ELN® offers a flexible, adaptable electronic lab notebook that supports diverse experimental needs. The platform’s Scientific Data Cloud consolidates instrument and research data enterprise-wide, paving the way for AI-driven insights. By unifying these components, Sapio simplifies data management and boosts productivity across the lab lifecycle. The platform is accessible for a wide range of industries and research applications. It aims to reduce administrative burden and enhance collaboration within scientific teams.

Quantib Brain is a radiology software solution that has received FDA clearance and CE marking, specifically designed for the segmentation of brain scans. Collaboratively developed with GE Healthcare, it operates as a plug-in for the Advantage Workstation (Server), delivering automated quantification of brain structures in a user-friendly software setting. This innovative tool allows for the longitudinal analysis of brain volume measurements, encompassing white matter, grey matter, intracranial volume, and cerebrospinal fluid, which aids in monitoring the progression of atrophy. Furthermore, it includes functionality for the segmentation and tracking of white matter hyperintensities. Quantib Brain offers a detailed summary of volumes for grey matter, white matter, ICV, CSF, and total brain volume, all presented in a clear results table. Users can also benefit from self-selected cross-sections, which can be easily exported into a detailed report, ensuring all examination findings are readily shareable for collaborative review. This capability enhances the overall efficiency of diagnosis and patient management in clinical settings.

Speeding up the creation of crucial medications and ensuring that patients worldwide can access top-notch cancer treatment and research equally. Our technology is transforming how patients access cutting-edge medicines and participate in clinical trials. FICS is a groundbreaking software solution that facilitates the gathering of regulatory-compliant data throughout patient treatment. By integrating previously isolated and non-interacting applications into a comprehensive, seamless platform, FICS is making clinical trials more efficient, quicker, and of superior quality, ultimately enhancing patient outcomes in significant ways.

uMotif is an innovative platform for eCOA/ePRO and eConsent, aimed at enhancing both clinical and real-world research efforts. Created with input from patients, this platform offers unmatched engagement, significantly improving the speed, quality, and precision of data collection. Through the integration of uMotif's eCOA/ePRO system with real-time glucose monitoring, the platform achieved remarkable compliance rates during a comprehensive diabetes study across Europe. In another instance, an immunology trial benefited from the patient-focused eCOA/ePRO solution, enabling the sponsor to fulfill data requirements a full six months ahead of schedule. Additionally, in a CNS study mandated by the FDA, participants utilized their personal devices to provide submission-ready ePRO data, showcasing the platform's versatility. uMotif's commitment to a patient-first design philosophy emphasizes a deep understanding of the patient experience and the factors influencing their behavior. This expertise not only ensures the development of software that addresses patient needs effectively but also results in extraordinarily high engagement levels for study sponsors, fostering a win-win environment for both parties.

PowerScribe One represents an advanced radiology reporting solution that utilizes artificial intelligence to enhance both diagnostic precision and workflow productivity. By leveraging Microsoft Cloud for Healthcare, this platform automates key elements of the radiology reporting process, such as creating initial impressions and providing immediate clinical insights. Its innovative features, which include Smart Impression and AI-driven findings, empower radiologists to generate comprehensive reports more swiftly and with reduced mistakes. Additionally, PowerScribe One facilitates smooth connectivity with electronic medical records (EMR) and incorporates cloud-based speech recognition technology, leading to more accurate documentation. This combination not only streamlines the reporting process but also significantly contributes to better patient care and outcomes. Ultimately, the integration of these technologies positions PowerScribe One as a vital tool for modern radiology practices.

Riverain Technologies has developed ClearRead Xray, a suite of five applications that have received FDA clearance, aimed at improving the speed and precision of interpreting chest X-rays within healthcare settings, all without the need for extra equipment, procedures, or exposure to radiation. This innovative platform utilizes specialized suppression technology to create a clear view of the chest, which significantly aids in the swift and precise identification of cardiothoracic conditions. Among its standout features are the generation of bone-suppressed images that enhance visualization, the ability to spot potential lung cancer nodules, a decrease in the time required to read portable X-rays, automatic comparisons with previous examinations to emphasize changes, and compatibility across various imaging devices and protocols throughout the enterprise. Additionally, the ClearRead Xray Bone Suppress feature notably enhances soft tissue visibility by minimizing the presence of bone structures in digital images, thereby assisting radiologists in uncovering nodules that may have previously gone unnoticed. This comprehensive approach not only boosts diagnostic capabilities but also streamlines workflow in busy medical environments.

Realize Medical's Elucis is an FDA-approved extended reality platform that simplifies the segmentation of images, promotes collaboration among remote teams, and allows for procedural planning in a virtual reality space. Elucis is capable of handling an unlimited number of 3D and 4D CT and MR images, ensuring thorough project integration. It boasts cutting-edge image processing features, including both manual and automatic registration, as well as the display of images in 2D, 3D, and 4D formats. The platform’s segmentation tools are engineered for efficiency and user-friendliness, enabling precise measurement, cutting, and planning tasks directly in a virtual environment. Additionally, Elucis includes advanced 4D modeling capabilities that permit intricate segmentation of cardiac structures in mere minutes, regardless of the phase. Users have the flexibility to import 3D structure files from external sources and can easily export their work with a single click. Furthermore, the platform enhances teamwork by allowing multiple users to connect seamlessly with local or remote colleagues throughout the entire workflow, making it a versatile tool for medical professionals. This feature not only streamlines communication but also ensures that all stakeholders can contribute effectively to the project.

EvidentIQ's eCOA streamlines the collection of real-time, direct-from-patient data through an easy-to-use interface that facilitates sophisticated patient assessments, ultimately enhancing both the patient experience and the quality of the data gathered. Clients have the option to choose a complete, all-inclusive eCOA solution or to mix and match various components tailored to their specific needs. By scheduling a demo with our knowledgeable team, you can discover how to maximize the return on investment for your research studies. The eCOA platform merges data science services with technology to provide a versatile solution. It operates independently of particular eClinical technologies like EDC systems, while also offering seamless integration with existing eClinical software ecosystems. Designed to efficiently gather a wide range of outcome data reported by patients, clinicians, or observers, this solution ensures compliance and enhances the overall data collection process. With such flexibility, organizations can adapt the eCOA framework to suit a variety of clinical trial scenarios, enhancing their research capabilities significantly.

Radiolens is an innovative PACS radiology workflow solution powered by AI that enhances diagnostic processes by automatically identifying low-quality scans and generating preliminary reports for various common modalities. This system promotes clinical collaboration and improves workflow efficiency, leading to better-informed decision-making. It features automated task assignments to optimize workload distribution and provides actionable insights that are both quantitative and qualitative, enhancing the speed and accuracy of reporting. Additionally, it includes a lightweight DICOM Viewer that allows users to access cases from mobile devices, thereby eliminating the need for on-site presence with its cloud-based solution. Users receive real-time notifications on their devices, ensuring timely updates. With top-notch accuracy, unlimited image backup, and straightforward archiving capabilities, Radiolens also delivers instant AI-evaluated biomarkers for essential qualitative and quantitative metrics such as CCAP diameter, listhesis, compression fractures, IV disc height, and thecal sac measurements. Its intelligent server automatically matches templates to studies based on the patient's gender and the modality being used, streamlining the workflow further. This comprehensive approach not only enhances the efficiency of radiology departments but also significantly elevates the quality of patient care.

OnePacs is a comprehensive, cloud-driven platform designed for teleradiology practices, imaging centers, hospitals, clinical trials, and healthcare networks, providing accessible PACS, RIS, and structured reporting solutions. Created by radiologists with the needs of their peers in mind, it streamlines modality workflows and facilitates image transmission while offering FDA-approved diagnostic viewing, secure storage options, archiving, disaster recovery, and automated structured reporting alongside voice recognition capabilities. The platform features a unified interface known as “OneWorklist,” which aggregates studies from various locations, ensuring a seamless user experience. With support for multi-user access that is location-independent and an impressive 99.99% uptime, OnePacs is also compatible with HL7/EMR systems, adheres to HIPAA regulations, and includes advanced peer-review tools along with quality assurance modules. Additionally, CaseLink enables secure sharing of cases among professionals, while its high-performance web DICOM viewer provides quick, mobile, and desktop diagnostic accessibility. OnePacs guarantees a swift implementation process—often completed in less than two weeks—while being scalable and backed by reliable 24/7 customer support based in the US, ensuring that users can operate efficiently at all times. This robust platform not only enhances workflow but also significantly improves the overall quality of patient care in various healthcare settings.

The L7 Enterprise Science Platform (L7|ESP®) is a comprehensive platform designed to contextualize data and remove business silos through process orchestration. This all-in-one solution supports the digitalization of data and scientific processes within life sciences organizations. It includes native applications like L7 LIMS, L7 Notebooks, L7 MES, and L7 Scheduling. L7|ESP seamlessly integrates with third-party applications, lab instruments, and devices to consolidate all data into a unified model. Featuring a low-code/no-code workflow designer and numerous pre-built connectors, it ensures rapid implementation and full automation. Utilizing a single data model, L7|ESP enhances advanced bioinformatics, AI, and ML to provide new scientific and operational insights. L7|ESP addresses the data and lab management needs and challenges within the life sciences sector, specifically targeting: ● Research and Diagnostics ● Pharma and CDMO ● Clinical Sample Management Explore the L7 Resource Center for on-demand recordings, case studies, datasheets, and more: l7informatics dot com/resource-center

Popsipen represents a groundbreaking advancement in Digital Pen and Paper Technology, enabling the seamless capture of handwriting and its transfer to a database through USB or Bluetooth connectivity. This device is as simple to operate as a traditional pen, offering a highly user-friendly method for real-time secure data transfer on a worldwide scale. Our organization stands out with a distinctive profile as a Contract Research Organization (CRO), uniquely fusing the implementation of clinical research with the creation of tailored IT solutions specifically designed for the pharmaceutical sector. Our adaptability and extensive experience in the pharmaceutical arena, all while prioritizing cost-efficiency, set us apart from other CROs in the industry. We pride ourselves on our ability to swiftly adapt to the evolving needs of studies, eliminating the cumbersome bureaucracy and delays often associated with conventional CROs. This flexibility allows us to deliver timely results without sacrificing quality, further enhancing our reputation as a leader in our field.

Embark on a journey towards enhanced data integrity and assured decision-making with Clinical Ink. As trailblazers in the realm of eSource, their technological framework and service offerings ensure increased reliability from the initial source all the way to submission. Discover Lunexis™, a well-defined and interconnected eSource Ecosystem that provides targeted data capture solutions tailored to your protocol during the pivotal moments that count. The Lunexis platform simplifies the deployment of a cohesive and user-friendly eSource solution, granting you access to your study data anytime and anywhere. We offer more than just rapid and accurate data; we instill assurance in your processes. With this approach, both your sites and patients benefit from a smoother experience, leading to improved patient compliance and engagement, as well as ensuring proper protocol execution. Take the first step toward successfully managing your most intricate studies with confidence — utilize Lunexis to facilitate informed and optimal decision-making for your research endeavors. Moreover, this innovative platform not only streamlines processes but also enhances collaboration among all stakeholders involved in the study.

NeuroQ stands out as a premier software for brain imaging analysis, delivering a robust diagnostic resource applicable across various modalities and clinical scenarios. This comprehensive tool supports an array of imaging techniques, including FDG, Amyloid, SPECT, DaTscan, and Epilepsy, thereby enhancing diagnostic precision in differentiating between various conditions. As one of the most prevalent quantitative instruments utilized in the differential diagnosis of dementia, NeuroQ transcends simple visual evaluations by offering crucial, objective diagnostic insights. It efficiently assesses metabolic levels across over 240 predefined brain regions, contrasting them with a normative database to quantify the extent of abnormalities and their statistical significance. Designed to assist in the evaluation of human brain scans, NeuroQ meticulously quantifies mean pixel values within standardized areas of interest and allows for detailed comparisons with other brain images, ultimately contributing to better patient outcomes. This innovative software is essential for clinicians seeking reliable data to inform their diagnostic processes and treatment decisions.

cubeCTMS is an all-encompassing clinical-trial management platform that facilitates complete oversight of trials, encompassing aspects such as tracking study sites and investigators, managing enrollment and visit schedules, and overseeing budget and contract workflows, as well as milestone reporting and document management. By centralizing study operations and automating essential processes, it allows sponsors, CROs, and study teams to oversee progress in real time, coordinate tasks across various studies, enhance communication with sites, and reduce risks. The platform offers integrated dashboards, notifications, and audit-ready documentation to ensure compliance with regulatory standards, including readiness for FDA 21 CFR Part 11, empowering stakeholders to oversee trial timelines, resources, and overall performance from a singular interface. Additionally, cubeCTMS seamlessly connects with other CRScube modules, such as EDC, eTMF, and pharmacy/RTSM, creating a cohesive ecosystem that minimizes redundancy, optimizes data flow, and supports flexible workflows during amendments or large-scale implementations. This integration not only streamlines processes but also enhances the overall efficiency of clinical trials, making it an invaluable tool for research teams.

Signant Health operates as a worldwide leader in evidence generation, striving to transform the landscape of clinical trials by connecting with patients in their environments and rethinking the route to validation. Their extensive range of clinical technology solutions includes electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician evaluations, and a cohesive eClinical platform. Additionally, they offer patient engagement solutions featuring a user-friendly app, eConsent for informed consent processes, and telemedicine functionalities. Furthermore, Signant Health delivers clinical data and analytics services, which include COA data analysis as well as the aggregation and interpretation of data. With a rich history spanning over three decades, they have played an instrumental role in supporting numerous trials and have been pivotal in hundreds of drug approvals, establishing themselves as a reliable ally for sponsors and CROs eager to provide high-quality data for informed trial decisions and regulatory submissions. Their commitment to innovation continues to shape the future of clinical research.

Modern Interactive Response Technology (IRT) systems are becoming more intricate. The significance of flexible and customizable IRT cannot be overstated, as this technology serves as the primary source for essential data, including recruitment metrics, clinical trial attrition rates, patient attendance, and more. It is vital to select a platform that is intuitive, optimized for mobile use, and all-encompassing—underpinned by high standards of quality, adaptability, and expertise. Embrace a partnership that offers profound therapeutic knowledge tailored to the contemporary risk-based eClinical landscape. By merging advanced technology with specialized knowledge and a dedication to exceptional service, we enhance clinical trials to achieve favorable patient results. Our extensive understanding of clinical processes and supply chain dynamics fosters innovation, granting clients greater control over their Randomization and Trial Supply Management (RTSM) protocols. Our cutting-edge tools elevate quality assurance, improve site productivity, and enhance patient adherence significantly. Furthermore, our IRT platform is adaptable enough to cater to a wide array of studies, with the capability for full validation and deployment in just 30 days, ensuring efficiency in clinical trial operations. This swift implementation can lead to more timely data collection and improved overall trial management.

Apollo Medical Imaging Technology is a pioneering software company focused on enhancing medical imaging through innovative image processing solutions tailored for both clinical and research purposes. Their leading product, MIStar, stands out as a cost-effective and user-friendly software suite that encompasses a wide range of advanced features and versatile cross-modality solutions, catering to the needs of clinicians and original equipment manufacturers alike. MIStar efficiently accommodates several imaging modalities, including CT, MR, NM, and PET, and boasts specialized modules such as CT Perfusion for stroke and various tumors, DSC-MRI for stroke analysis, DCE-MRI for tumor assessments, as well as DWI & ADC, and DTI Fiber Tractography. Additionally, it offers NM Renogram Analysis and Image Fusion capabilities, making it a comprehensive tool in medical imaging. The software also ensures seamless data management and image input via DICOM networking, complemented by an intuitive clinical database that facilitates easy anonymization and archiving of sensitive patient data. This combination of features positions MIStar as a crucial asset in modern medical imaging practices.

Uncover the most cutting-edge methods in the realm of clinical and patient-reported outcomes data. Our comprehensive solution transcends mere data entry, facilitating a genuinely patient-focused research experience. While our eCOA software is deeply rooted in principles of behavioral science, it has also been designed specifically by healthcare professionals to align with the needs of both sites and sponsors. By emphasizing personal identity, motivational intervals, and significant objectives, we stand out from other eCOA solutions. The Datacubed app features a user-friendly interface that allows participants to quickly engage with what truly matters. It has been highlighted that gathering data is now more straightforward than ever, thanks to our adaptable, user-friendly, and interactive application. As the need for flexibility in trial design continues to grow, we provide versatile data collection options that can be executed in person, remotely, or as a hybrid approach, catering to the diverse requirements of traditional, hybrid, and virtual clinical trials. This adaptability ensures that researchers can effectively capture the most relevant data, regardless of the study format.

Enhance your team's capability to make informed decisions that not only improve IT operations but also positively affect patient outcomes. With seamless integrations and top-tier data security protocols, data can be accessed from various locations, devices, and portals. By eliminating outdated migration tools and consolidating vendors, you can achieve significant cost savings and efficiency improvements through a unified imaging network. Silverback evolves with each data interaction, becoming increasingly intelligent and efficient. Over time, its engine recognizes and monitors patterns, providing predictive insights across the image network. At the core of the Silverback platform, Vue serves as an adaptive DICOM router that smartly directs studies throughout the organization. This router skillfully manages images for diverse sites and vendors using tailored logic rules. Vue can be strategically positioned either in front of the PACS or behind the modalities, ensuring optimal capture, management, and distribution of studies across the entire network. Embracing such innovative technology can lead to more streamlined workflows and better healthcare delivery.

IntelliSpace Portal 9.0 is an innovative visualization platform encompassing over 70 clinical applications, providing a cohesive solution that enhances speed and efficiency while boosting diagnostic confidence, particularly in the analysis and monitoring of complex cases. As the global population ages, the prevalence of neurodegenerative diseases continues to escalate, necessitating long-term monitoring for patients with neurological disorders, which can often exhibit subtle brain changes that are difficult to identify. To address these challenges, IntelliSpace Portal 9.0 introduces several new and improved neuro applications, including NeuroQuant®¹, LoBi, and CT Brain Perfusion, all designed for swift, objective, and consistent image assessment. Additionally, with a growing focus on pulmonary health, this platform equips you with a comprehensive suite of tools to seamlessly manage pulmonary disease from initial detection through to ongoing follow-up, ultimately aiming to improve patient outcomes. This integration of neuro and pulmonary features positions IntelliSpace Portal 9.0 as a vital resource in modern medical imaging and diagnostics.

Silhouette® offers a comprehensive range of tools for imaging, three-dimensional measurement (including both depth and volume), and the documentation of soft tissue and skin lesions such as wounds. It is FDA cleared, adheres to HIPAA regulations, and includes integration capabilities with electronic medical records. Among its advantages, the system is tailored for both clinical trials and everyday clinical use, featuring a variety of devices designed to accommodate diverse user requirements throughout the continuum of care. Users can choose from both wired and wireless 3D imaging devices, as well as applications for mobile devices, ensuring that each site and user can find the right fit for their needs. This innovative solution facilitates the capture of images, depth measurements, data analysis, and reporting within a single, user-friendly, and secure platform. The centralized database, known as SilhouetteCentral, allows multidisciplinary care teams and risk managers to access and analyze captured data instantly and securely from various locations. By delivering exceptional precision and consistency in data collection, Silhouette® significantly mitigates risks associated with inaccuracies in medical documentation and enhances the overall quality of care. In this way, it ensures that healthcare professionals can rely on accurate data to inform their treatment decisions.

Clinevo's electronic Trial Master File (eTMF) is a user-friendly digital solution for the organization and storage of documents, images, and various digital assets related to clinical trials. This eTMF incorporates an integrated DIA reference model and complies with regulatory standards. Additionally, Clinevo offers the MICC Intake, a web-based platform designed for Medical Information Call Centers (MICC) and Pharmacovigilance (PV) professionals to efficiently log, track, and monitor Product Quality Complaints (PQCs), Medical Inquiries (MIs), and Adverse Events (AEs). Furthermore, Clinevo Safety serves as a comprehensive cloud-based system that ensures ease of use and regulatory compliance throughout the entire Pharmacovigilance process, encompassing PV Intake, Case Processing, Regulatory Submissions/AS2 Gateway, Analytics, and Safety Signals, all within a single platform. Lastly, the Clinevo Website Intake tool can seamlessly integrate with Sponsor or CRO websites, offering consumers and reporters an intuitive web interface for easy access and reporting. This innovative suite of tools enhances the efficiency and effectiveness of clinical trial management and safety reporting.

Ibex Medical Analytics stands at the forefront of AI-driven cancer diagnostics within the field of pathology. Our diverse team comprises entrepreneurs, data scientists, software engineers, and medical professionals united in our mission to revolutionize cancer diagnostics through artificial intelligence, ultimately enhancing patient care. As the volume of tests continues to rise annually, pathologists face significant challenges in delivering precise and timely analyses. To address this, Ibex harnesses the power of AI to create clinical-grade solutions that aim to identify cancer with the same level of accuracy as a human pathologist. The Galen Platform employs advanced algorithms to scrutinize images, detect and classify cancer in biopsy samples, and highlight other clinically significant findings, thereby assisting pathologists in minimizing diagnostic errors while streamlining their workflow. Notably, Ibex’s Galen™ Prostate and Galen™ Breast solutions represent the pioneering AI-based cancer detection tools integrated into routine clinical practice in pathology labs, showcasing proven efficacy in uncovering previously missed cancer cases. As we continue to innovate, our commitment to improving cancer detection and patient outcomes remains unwavering.

RedBrick AI serves as a rapidly collaborative platform for annotating medical data, specifically designed to assist healthcare AI teams in creating high-quality training datasets across various types of radiological imagery, including CT, MRI, X-ray, Ultrasound, Fluoroscopy, and additional standard imaging techniques. The platform is adept at managing intricate tasks such as multi-series annotation and extensive DICOM studies, thanks to its native compatibility with medical data formats including DICOM and NIfTI. Furthermore, it boasts cutting-edge, user-friendly 2D and 3D web-based annotation tools, complemented by a PACS-like viewer. RedBrick AI supports a wide array of annotation use cases, including instance and semantic segmentation, landmark identification, classification, and ROI measurements, thereby enhancing the speed of annotation processes by as much as 60%. This significant improvement in efficiency can empower healthcare professionals to focus more on patient care rather than on time-consuming data preparation tasks.

The INFINITT Cardiology Suite serves as a comprehensive platform that consolidates all cardiovascular information into a single solution, enhancing the management, analysis, reporting, and submission of images to various data registries. Furthermore, it has received certification from the American College of Cardiology (ACC), confirming that version 1.0.8.1 of the INFINITT Cardiology Suite complies with the NCDR standards for the CathPCI Registry® version 5. This suite functions as an online PACS and reporting tool tailored for cardiology and vascular imaging, as well as EKG and nuclear medicine applications. It can operate independently or integrate seamlessly with INFINITT PACS, thereby unifying data for electronic health records (EHR). Users can customize report templates that are compatible with Dragon Dictation, allowing for flexibility and efficiency. Additionally, the suite offers both basic and advanced measurement tools for echocardiography, non-invasive vascular imaging, EKG, nuclear medicine, and cardiac catheterization studies. It provides sophisticated report generation capabilities, including the automatic population of measurements and interpretations, which significantly reduces transcription expenses and enhances workflow efficiency. This integration leads to improved patient outcomes through timely access to comprehensive data.

CSAM Picsara serves as a comprehensive image management system that facilitates real-time image capture, storage, and archiving. This innovative solution boosts the precision and quality of image documentation, leading to improved accuracy and care. Many of Sweden's largest hospitals have adopted CSAM Picsara for its user-friendly interface that addresses all aspects of image management within healthcare organizations. Its compatibility with a wide range of medical devices and media types makes it adaptable for various medical fields. Additionally, CSAM Picsara plays a vital role in the seamless sharing of clinical images, which is essential for accurate diagnoses and maintaining complete patient records, thus ensuring high-quality patient care. With this system, patients can transition between healthcare professionals or departments without the risk of their medical information being lost. Moreover, CSAM Picsara enables healthcare providers to effortlessly share extensive digital information, while users can easily store relevant annotations and measurements alongside images or videos within patient files. This functionality not only streamlines workflows but also enhances collaboration among medical teams.