Alternatives to QMENTA

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.

We simplify the complexity of managing your product lifecycle. The STARLIMS brand of laboratory informatics solutions is easy to use and adaptable to the needs of your organization. Our laboratory information management software (LIMS) can be integrated with your existing systems and can identify opportunities to improve processes to help you bring high-quality, safe products to market quicker.

Three Palm Software's breast image workstation product1 called WorkstationOne offers a distinct style of enterprise integration workflow and interpretation. Three Palm Software is aware of the data-intensive challenges radiologists face when they move to digital mammography and the need to review mammograms digitally as efficiently as reading films on motorized lights. This mammography software's elegant, simple interface is designed to meet even the most demanding radiologists. Tabar's systematic mask viewing techniques* are used to search for subtle radiographic anomalies. Full-resolution images can be viewed using the mouse wheel, with a visual trace of pixels viewed. No need to manually pan or zoom to see all pixels in full resolution.

Clario's Imaging Platform provides accurate results for complex clinical trials. It is secure and streamlined. Our in-house medical expertise combined with our proprietary imaging systems allow us to customize your workflow and analyze it to your specific needs. Our engineering teams remove the additional cost and time that comes with relying upon third-party systems. Clario is the leading Imaging Core Lab in the world, with more than 30 doctors and 35 scientists devoted to medical imaging. Our decades of experience in reviewing and assessing medical images has informed the development of our proprietary imaging systems. Clario's SMART Submit app incorporates this expertise from the moment it screens a medical picture for errors at the hospital to the final image interpretation.

Version 8.0 of PDQuest 2-D analysis software offers flexible and comprehensive 2-D gel electrophoretic analysis. PDQuest Basic is for basic 2-D gel analysis, while PDQuest Advanced provides the most recent features for 2-D Gel-Based Expression Proteomics Studies. The advanced analysis tools can reveal subtle differences between 2-D gels, regardless of whether you choose the basic or the advanced version. The powerful auto-matching algorithms match gels quickly and accurately with minimal or no manual intervention. Flexible annotation features in PDQuest software make it a useful tool for creating a centralized information repository that allows virtually any type or characterizing data to link to each spot on a master image. It is easy to access and share information about identified proteins. Spot cutting configurations allow for high throughput and flexibility in protein identification experiments.

The industry's best AI-powered clinical analytics platform provides actionable insights that enable your teams to manage risk, improve performance across sites, studies, and vendors. Saama's state-of-the art clintech is designed to streamline workflows, automate tedious processes, and improve collaboration across clinical operations. Saama is trusted by sponsors and CROs for data aggregation, artificial intelligence solutions, and improved decision-making. This can help to reduce drug development costs and timeframes, as well as eliminate delays. Saama can help you get on the fast track for clinical trial process innovation. Your ClinOps and medical review team will find it much easier to access all of your clinical data in one place. Data managers are often undervalued. They can now focus on the data points that are important by eliminating manual work.

Inefficient document workflows can be eliminated, which can lead to a loss of time and money and a reduction in your ability to scale up and attract new research. Florence eBinders integrates your clinical trial systems, automates eRegulatory processes and tracks study progress. It also enables secure remote monitoring via the industry-standard eRegulatory and eISF platforms. Florence eBinders integrates your clinical trial systems. It automates eRegulatory processes and reduces time for contract negotiation. It also tracks study progress and allows secure remote monitoring. Our top-ranked implementation teams and support team will quickly set up your study and get all users connected. In less than four weeks, most sites are up and running. Secure access to your monitors and remote access for your team can reduce the time spent on site monitor visits.

Ambra Health, a cloud-based platform for image and medical data management, is designed for hospitals, radiology groups, contract research organizations, and medical groups. The Ambra Health software is intuitive, scalable, and highly interoperable. It allows healthcare providers to improve collaboration through image exchange with patients and departments. Ambra's secure storage solution allows users to save all imaging in one repository. It also allows them to store many types of medical imaging file formats, including TFF, JPEG and DOC. Core features include EMR/EHR integration, Cloud VNA integration, PACS integration and Cloud VNA. Telestroke, informatics first migration, and many more.

PowerServer™, a PACS that optimizes your imaging workflow, is the perfect choice. This web-based, customizable PACS allows imaging departments to instantly access patient images and reports whenever they need them. It allows unlimited licenses for users, modities, and facilities making it easier than ever to expand your business. This customizable solution allows imaging facilities and radiology departments to choose the best solution for them. PowerServer™, a cloud-based, hybrid or on-prem PACS, is available. Highlights: Built on a single web-based database platform Available as a cloud, hybrid or on-prem option Templates that can be customized QR SNAP allows for easy image sharing RapidResults™, a powerful zero-footprint viewer Voice recognition (add-on)

Online scheduling and room management that is intuitive, intuitive, and rules-driven to simplify patient bookings. It's fast and almost error-free. Automated scheduling of complicated segments. Efficient, paperless patient registration and document administration. Online, real-time online insurance verification. You can manage multiple facilities at once. Integrated auto CDS tool. The Q/ris technologist workflow module not only automatically captures DICOM SR data but also contains a wealth of tools that will help your technologist prepare data-rich studies and save time for you. Automatic generation of exam-specific electronic sheets for technologist notes or annotations. Any time, real-time editing, modifying and rescheduling exams. Interactive supply capture and automatic charge capture. Worklist for MIPPS compatible DICOM modality. Automatically capture DICOMSR data from the modality.

Streamline regulatory operations within your organization to improve compliance. Veeva SiteVault simplifies clinical trial management by connecting all regulatory operations. This improves efficiency and compliance. A single system that integrates regulatory and source documents supports 21 CFR Part 11 compliance and HIPAA requirements. SiteVault Enterprise provides real-time visibility across trials and speeds study activation. It also enables faster and more quality trial execution. To speed up study activation and reduce manual work, you can replace manual processes with your own workflows. Monitors will have secure, direct access into your source and regulatory documents. This will eliminate the need to redact or grant EMR access. You can create your own workflows, reports and dashboards to gain greater insight into regulatory processes and start-up timelines.

Disks from outside organizations are flooding hospitals and imaging centers. Manual import of data can be very time-consuming and costly. Automated Disc Importer allows organizations to import large volumes of discs into local or temporary cloud storage. This automates the process and eliminates the need for human intervention. After discs have been read, users can reconcile the data and then import it into their archive. The Automated Disc Importer takes a photo of each disc label being read to provide additional security. The photo clearly identifies the disc's origin. Automated Disc Importer ingests reports and medical images from DICOM discs. This drastically reduces the time required for manual importing.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

Dragonfly is flexible, powerful, and user-friendly. It provides quantitative answers to today's most challenging 2D/3D/4D imaging questions, including data from correlative, hyperspectral imaging systems and X-ray, SEM and FIB-SEM as well as data from confocal microscopy and other advanced applications. Interactive inspection tools and robust quantification workflows give you detailed insight into material properties and structures. Data restructuring, filtering and volume registration are just a few of the post-processing functions. Image stitching is another option. Use powerful segmentation tools to accurately label image elements. Dragonfly's Deep Learning solutions can help you solve image enhancement and segmentation problems. Easy-to-author macros make it easy to automate your 3D analysis workflows. Dragonfly with Deep Learning offers a transformative solution to image processing. Experience the only commercially-supported Deep Learning engine that lets you train and execute custom networks.

Ibex Medical Analytics is a pioneer in AI-powered pathology cancer diagnosis. We are a multidisciplinary group of entrepreneurs, data scientists and software engineers, who work together to realize our vision of transforming cancer diagnosis with AI and improving patient care. As the number of cancer tests increases each year, pathologists face increasing challenges in providing accurate and timely analysis. Ibex uses artificial Intelligence (AI) to create clinical-grade solutions that detect cancer as accurately and quickly as a human pathologist. Galen Platform uses algorithms that analyze images and grade cancer in biopsies. It also points to other clinically important findings. This helps pathologists reduce diagnostic errors and improve efficiency. Galen™, Breast and Galen™, Prostate are the first AI-based cancer detection solutions that Ibex has ever used in routine clinical practice in pathology laboratories. They have been proven to be able to detect missed cases.

IntelliSpace Portal 9.0 has over 70 clinical applications. It is an advanced visualization platform that allows you to work more efficiently and quickly, especially when it comes to reading and following up on multi-faceted cases.

TrialKit is a cloud-based platform available via both a web and native mobile app, enabling end-to-end clinical trial management for medical device, diagnostics, digital therapeutics, and biopharma companies of all sizes. Design and deploy validated studies in days not weeks using our intuitive study builder that requires no programming. Thousands of global users have leveraged the flexibility of TrialKit to deploy over 8,000 studies across all phases of development.

Radiolens, an AI-enabled PACS radiology workflow system, makes diagnostic workflows more efficient by automatically detecting low-quality scans and creating preliminary report for the most common modalities. It facilitates clinical collaboration, streamlines workflow efficiency, and allows for informed decision-making. Automated assignments for optimizing workload. AI-enabled qualitative and quantitative actionable insights to improve your reporting speed. You can use the lightweight DICOM Viewer to view cases from your mobile device. An on-cloud solution can remove restrictions on site presence. Receive real-time notifications directly to your device Maximum accuracy, Unlimited backup, and simple archiving of images. Instant AI-assessed biomarkers are available for qualitative and quantitative descriptions like CCAP diameter, compression fractures and IV disc height. Our intelligent server automatically matches templates to studies based upon patient gender and modality.

Unifier is an interoperable, powerful enterprise imaging platform that allows for seamless integration of health data. This results in better patient care and increased IT performance. Dicom Systems offers a wide range of enterprise imaging solutions that can scale with your business. The platform allows teleradiology workflows and intelligent routing. It also integrates with HL7 and SSL-based DICOM. AI on-ramp is available. Enterprise-class vendor-neutral archiveing is possible. Route by any private or standard DICOM tag, date, time and cache data for later delivery. Interoperability with heterogeneous information systems, and all DICOM and HL7-enabled devices. To ensure study transfer, performs incomplete study delivery checks. WebGUI configuration tools that are transparent and user-friendly. Enterprise-wide configuration management, logging, and auditing for HIPAA.

CureMetrix harnesses the power of Artificial Intelligence to improve cancer survival rates and disease detection. We believe that radiologists will benefit from the latest technology in mammogram evaluations. This will improve their clinical and financial outcomes, as well as provide greater assurance for hospitals and patients. Our algorithm has shown promising results in preliminary studies that have included thousands of images. This algorithm is capable of reducing false-positive rates, which can lead to unnecessary follow up procedures and undue anxiety among patients. We are working on a powerful technology that will allow health care providers to pinpoint even the most minute changes faster and more accurately than ever before. Our image analysis platform is being designed to improve mammography's ability to evaluate dense breasts.

EvidentIQ's eCOA optimizes real-time, direct from-patient data collection. It offers a simple interface that provides advanced patient assessments to improve the patient experience and data quality. Customers can either benefit from an entire eCOA package, or choose the elements that meet their specific needs to create value. Get a demo from our experts to see how we can help you improve your study ROI. EvidentIQ's eCOA brings together data science and technology. Customers can either benefit from an entire eCOA package that covers all aspects of the process or add value by choosing elements that meet specific requirements. The solution can be used independently of any specific eClinical technologies, such as EDC systems. However, it can be integrated into any existing eClinical software. It has been created to collect any patient/clinician/observer reported outcome data in a streamlined, compliant and efficient way.

The Interactive Response Technology (IRT), systems of today are becoming more complex. Flexible and configurable IRT is important - IRT data can be used as the source of record to recruit, drop-out rates in clinical trials, patient visits, or any other vital data. You want a platform that is user-friendly, mobile-ready and comprehensive. It should also be embedded in quality, flexibility, and expertise. In today's risk-based eClinical environment, comfort is combined with complex therapeutic expertise. We empower clinical trials to deliver positive patient outcomes by combining the right technology, subject matter knowledge and a commitment to service. Clients have control over their Randomization and Trial Supply Management processes (RTSM) thanks to deep clinical and supply chain knowledge. Our innovative tools drive exceptional levels of quality control, site efficiency, and patient compliance. Our IRT platform is able to meet the needs for almost any study and allows fully validated deployment in as little time as 30 days.

Clinevo electronic trial master file (eTMF), is an electronic Trial Master File in electronic format (digital content). It can be used to organize and store documents, images and other digital content for clinical trials. Clinevo electronic Trial Master File eTMF has an inbuilt DIA reference model that meets regulatory guidelines.

ARIA®, an oncology information system, supports medical and radiation therapy, including proton therapy. You can review clinical images, prescriptions and lab results. Automate cancer staging based upon AJCC guidelines and manage toxicities easily. Interoperability is our focus. This allows you to make the most of patient information across platforms and devices. We provide extensive HL7 support and make it easy for patients to be transferred between hospitals. Your teams have instant access to patient data, allowing them to plan better and make adjustments as needed. We can help you optimize image-guided treatments using radiographic, fluoroscopic and cone-beam CT images. ARIA OIS records activities for evidence-based pay-for-performance programs and facilitates HIPAA compliance. ARIA organizes and stores patient data and images to help your teams stay focused and up-to-date.

IDBS Polar is the first BioPharma lifecycle management (BPLM) platform in the world. It eliminates repetitive manual tasks and allows you to execute your processes efficiently while curating data. This will allow you to accelerate the time to market, by tackling the most challenging challenges of process design, optimization scale-up and technology transfer. Interactive data analytics applications such as bioreactor comparision designed specifically for biopharmaceutical development scientists. IDBS Polar is an integrated platform that manages drug progress in contexts such as workflow, integration and insight. Workflows designed for the BioPharma lifecycle, with process-aware design, planning, and execution. Integrations that give meaning to your data. Rapid integration into your development environment, enabling automation, and curating a data backbone based on processes.

Dotmatics is the global leader in R&D scientific software that connects science, data, and decision-making. More than 2 million scientists and 10,000 customers trust Dotmatics to accelerate research and help make the world a healthier, cleaner, and safer place to live.

Silhouette®, a collection of products that can be used to image, 3D measure (including depth and volume), and document soft tissue and skin lesions. FDA cleared, HIPAA compliant, and integrates EMR. Benefits: This product is suitable for clinical trials and clinical practice. It also supports EMR integration.

Pulse is a cloud-based platform that allows echo labs to save time and improve the outcomes for their patients. Pulse is a cloud-based echocardiography reporting and storage solution. Access the information of your patients whenever and wherever you need it. Physicians can access their patients' information from almost anywhere. All you need to run an echocardiography lab. An elegant and powerful reporting interface that displays your images and measurements right alongside them. Fully automated, AI-powered GLS, LVEDV, LVESV, and LVEF measurements without ever having a button to press. Cloud-native software offers all the benefits that cloud-native software has to offer. You can send finalized reports directly from your EHR via HL7 to streamline your clinical workflow. You can either store new studies directly in the cart or retrieve them from an external PACS. Easy VPN management is made easier by the built-in support of DICOM-TLS.

The CardioMotionTM software, available in Australia from CDN, changes the game. It changes the way that you support the rapid identification and treatment of cardiac issues. The software is intended for emergency medicine, CCU/ICUs, oncology departments and medical center clinicians. It can also be used in regional and remote sites that use point-of care devices. Also useful in cardiac monitoring for clinical trials. Merlin CardioMotionTM works with slow frame rate clips without an ECG trace to detect it. It is therefore suitable for use on clips from lower specification machines. Merlin CardioMotionTM uses proprietary algorithms to detect the ventricular walls and borders automatically. This is possible thanks to revolutionary image processing technology. This allows you to quickly and accurately assess the dynamic performance of your patient's cardiac system.

Deeplink Medical developed its offering around the MIRIO platform. This adapts to the various use cases and needs for actors involved in medical image in oncology, in clinics, and in routine. Our services are based on three complementary offerings, MIRIO, which is a platform for the monitoring of solid tumors and the treatment response of patients in oncology. The patient pathway is a link between hospitals and liberal medicine. An Imaging CRO is responsible for the monitoring of imaging data during oncological clinical trials. Our solutions are supported by a scientific board. A collaborative workflow platform that structures imaging data and radiological examinations for patients suffering from solid tumors. This allows structuration of data in real time (according to the RECIST 1.1 or iRECIST) at the initial creation of the data. Real-time evaluation of treatment response according to international guidelines RECIST.1.1 and iRECIST.

CSAM Picsara, a complete image management system, allows image capture, storing, and archiving in real time. The system improves precision and quality while also increasing accuracy and care. Many of Sweden's most prestigious hospitals use CSAM Picsara. CSAM Picsara, an easy-to use system that meets all organization's image management needs, is simple to use. It can be used with all types of medical devices and media. This makes it adaptable and suitable for every medical discipline. CSAM Picsara helps healthcare providers share clinical images that are vital for diagnosis and complete patient records. This allows for high quality care. Patients can easily transfer between departments and healthcare professionals without losing their medical data. CSAM Picsara makes it easy for healthcare professionals to share large amounts digital information. Annotations and measurements can be stored in patient cases.

Integrated enterprise imaging can help you deliver better care. You can simplify enterprise imaging with scalable solutions that improve care coordination across specialties, speed up clinical decision-making, as well as realize better financial outcomes. Our enterprise imaging solution suite offers a single platform portfolio that streamlines workflow, improves labor utilization, and reduces IT complexity. Cloud-native technology allows us to offer advanced applications, seamless efficiency, superior cybersecurity, data storage, and agile upgrades. Consolidating systems, eliminating redundant hardware and automating manual tasks can help reduce costs. Capturing unrealized billings from encounter-based examinations can increase revenue. Documenting clinical decisions and capturing billing evidence will improve compliance. You can reduce your IT footprint by eliminating redundancy, improving IT operations, and centralizing enterprise imaging on one platform.

INFINITT Cardiology Suite combines all your cardiovascular data into a single solution. This streamlines image management, analysis, reporting, and submission to data registry. INFINITT Cardiology Suite v. 1.0.8.1 has been certified by American College of Cardiology (ACC). This certification demonstrates that INFINITT Cardiology suite v. 1.0.8.1 meets NCDR standards for version 5 of CathPCI Registry®. INFINITT Cardiology Suite INFINITT Cardiology Suite provides a web-based PACS system and reporting system for cardiology, vascular imaging, nuclear medicine, and other medical disciplines. It can be used independently or integrated with INFINITT's PACS to consolidate data for the EHR. Report templates can be customized and are compatible with Dragon Dictation. Advanced and basic calculations for echocardiography and non-invasive vascular, nuclear medicine, and cardiac catheterization images. Advanced report creation with auto-population and interpretations. Reduce transcription costs

RedBrick AI provides a platform for rapid and collaborative annotation of medical data. Platform designed to help Healthcare AI teams create high-quality training data for all types radiological imaging including **CT/MRI, Xray, Ultrasound and Fluoroscopy. With native support for medical formats such as DICOM, NIfTI, and other standard imaging, it can handle complex tasks such as multi-series annotating and extensive DICOM study. Our platform offers the most advanced and intuitive 2D & 3-D web-based annotating tools, with a PACS like viewer. All common annotation use-cases such as instance/semantic segments, landmarking and classification, as well ROI measurements are supported. This can accelerate annotation by up 60%.

Arterys, the AI platform for medical imaging, allows you to integrate leading AI clinical applications into your existing PACS/EHR driven workflow. This makes it an extension of what you do already. AI is real. We improve physician experience, accuracy in diagnosis and treatment, financial performance, and outcomes that are important to patients and providers. Accessible from any valid device via the cloud, it is fast and easy to deploy. There is no need for PHI exchange. It is completely secure. Arterys can be connected to your PACS/RIS/EMR/dictation software. Rapid deployment with minimal infrastructure. Available in over 100 countries. Our elastic cloud GPU architecture speeds up all tasks. You can render 3D files, large multi-dimension data in Gb and run multiple AI applications simultaneously. Image caching and pre-fetch allow for faster loading and analysis.

SenseTime's SenseCare Smart Health Platform combines cutting-edge AI algorithms with advanced image post-processing technology to provide high-performance diagnosis and treatment assistance solutions. The platform is based on medical big data and aims to provide smart tools to various clinical departments to support the entire process for diagnosis, treatment, and recovery. It also helps improve the efficiency and accuracy in diagnosis and treatment planning by doctors. SenseCare allows seamless connection to existing CT/MRI/Xray equipment and PACS without interfering in the original workflow process of hospitals. Using the same hospital's web browser, multiple users can log in to the platform and perform analysis on different portable devices. This platform can perform a variety of 3D post-processing, such as: This platform supports the entire workflow of diagnosis and treatment, as well as rehabilitation.

Popsipen is a unique Digital Pen and Paper Technology. It captures handwriting and then transfers it to a database using a USB or Bluetooth connection. This device is as easy to use and intuitive as a regular pen. It allows you to transfer secure data on a global scale in real-time, using a Bluetooth or USB connection. Our unique profile is that of a CRO that combines clinical research implementation with the creation of IT applications tailored to the pharmaceutical industry.

Our mobile visualization platform, which has won awards, allows healthcare professionals to collaborate and share 2D/3D medical images from any device. Secure access to data anywhere without the need to copy or move any source files. Trusted by the most advanced healthcare institutions around the world, ResolutionMD has been selected. The ResolutionMD enterprise viewer was created by clinicians for clinicians. It streamlines workflows and improves patient care. You can diagnose on mobile and the web with confidence using FDA Class II and other international accreditations. PureWeb®, a software development platform, powers ResolutionMD.

eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.

One platform to research, document, and collate your clinical data. The Nucleus platform simplifies research data. One platform to store all your study documentation, clinical data, submission data, and compliant media. Nucleus Documents allows you to manage and control your media and quality documentation. You can easily manage, control, and share company content. Our centralized regulatory document management solution makes it easy to manage and collect electronic trial master files. Nucleus Coding allows you to code dictionary terms against both WHODrug and MedDRA dictionaries. It can be used in our standalone application or integrated into your data capture software.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

Clinpal is the first platform for clinical research that is designed to allow virtual, hybrid, and direct-to patient studies. Patients can log in from any device, at any time. The trial's entire life span is managed by study teams that use powerful data and analytics. Sites also have all the functionality they need, which reduces burden. Clinpal Build is a point-and click studio that allows CROs and other users to quickly and easily define data, forms, and workflows. Clinpal's Single Platform provides complete clinical trial support, from patient recruitment through data capture and long-term follow-up. Data is available on-demand. Clinpal's innovative technology - Clinpal can be used in multiple formats with one online configuration. Clinpal works on all devices, including mobile and app users.

TCS ADD platform speeds up speed-to-market for the pharmaceutical industry across all clinical R&D value chains and makes clinical trials more efficient and safer. TCS ADD facilitates digital ecosystems, simplifies data complexity, and provides patients faster access to effective drugs. The platform is powered with TCS Decision FabricTM cognitive artificial intelligence engine, smart analytics and IoT which provides superior business value for the pharmaceutical industry. The next-generation, end-to-end metadata-driven solution for managing industry and sponsor clinical standards. Data science-driven platform that uses AI & ML technologies to speed up study start-up, targeted interventions, and quicker decisions. This solution digitizes the entire clinical supply management process, while placing the patient at the center. This increases patient safety and overall efficacy.

Clinical Ink is your guide to making confident decisions and obtaining cleaner data. Clinical Ink is a pioneer in eSource. Their technology platform and delivery capabilities give you greater certainty from source through submission. Explore Lunexis™, a connected eSource Ecosystem that provides data capture solutions tailored to your protocol at the crucial moments that matter. Lunexis makes it easy to create an integrated, simple eSource solution that gives you access to your study data from anywhere, anytime. We offer more than fast, reliable data. We also provide confidence. Your sites and patients will have a smoother experience. You can also be sure that your patients will be more cooperative and engaged, and that your protocol will be executed correctly. Lunexis can help you make informed, optimal decisions when you start the most complicated studies.

Medable is a software platform that allows you to conduct clinical research and studies. The software actively involves patients, who can be contacted remotely, in order to obtain the best results. Remote consent can be given by patients for digital examinations. The application also adapts to local regulations and languages. Our flexible, modular digital platform and DCT platform allows you to right-size how your protocol will be decentralized. Remote screening at scale worldwide Meet your studies enrollment targets faster. Any screening assessment can be developed. Responsive layouts on mobile and web can improve consent readability. Remote consent can be delivered to patients in a manner similar to consumer digital experiences. Global flexibility and local regulations can be accommodated. Engage patients and reduce the travel and time required for an on-site visit. Increase patient engagement and access.

TrialStat, in comparison to other EDC tools on the market such as MediData, DataTrack and Omnicomm, is the most comprehensive suite of study management tools. It can seamlessly connect to external data sources like EMR, wearables and other clinical and nonclinical data and information sources. TrialStat is a fully integrated platform that can be used for all types and phases of trials. Our multi-tenant, single-sign-on EDC suite includes modules to randomize, adjudicate, code, safety, patient diaries/ePRO and Vendor Neutral Imaging Archive. It also has a robust Reporting and Analytics Portal and custom Machine Learning programmes. TrialStat focuses on data analytics and provides real-time reporting, data extractions on demand and analytics across a single study or a program. This gives all stakeholders timely, relevant, customized insight into all aspects and highlights areas of risk or potential delays.

Sehat Central HMIS, a unique, standardized and secure cloud-based platform that allows healthcare professionals to streamline their practice workflow at hospitals, clinics, labs and diagnostics centers, is an intelligent, secure, secure, cloud-based platform. Integrate OPD, IPD Lab, Pharmacy, Radiology departments seamlessly.

We create solutions that connect and empower clinical trial ecosystems. The Enrollment Performance Monitoring platform that sponsors love and sites rely on. It is used by over 2,000 research sites in 26 countries, and half of the top-20 global biopharma firms. Sites are able to move patients forward by spending less time on redundant and manual tasks. Sites do less double work. Sites and sponsors will have fewer logs, phone calls, emails, and emails. With real-time access and real-time data, sponsors can optimize enrollment. It is simple and easy to use, with over 1,800 sites in 26 countries using it for patient recruitment. To run more predictable and faster clinical trials, access powerful enrollment and recruitment insights. You can stop wasting time and get back to what matters most: helping patients. You can manage recruitment across all sponsors, trials, and CROs. Once you enter information, it will go where you need.

AI products integrate seamlessly into your PACS or radiology workflow, allowing radiologists to automate tasks while providing efficient patient care. Radiologists are drowning because of the increasing demand for medical imaging in healthcare. This often leads to increased reporting errors, high workload, and a cluttered workflow. Radiologists can automate many of their repetitive tasks using AI. It also identifies standard measurements and allows them to generate high-quality reports that are evidence-based. This will allow referring doctors and physicians to make more confident decisions based on accurate data and a more intuitive workflow. Identify, characterize, and classify key elements with the highest accuracy. The images are loaded quickly and with no loss of quality. Smart suggestions are available in the template search. You can use pre-filled illustrative templates for your report or quickly customize them for standard clinical communication.

Image exchange via FTP, VPN, and CD is a problem for imaging centers today. It reduces their efficiency and makes it harder to compete with companies who have changed their image exchange model. The PACS & Teleradiology solutions by EthosMed allow users to consolidate, share and exchange images with providers in real-time. This results in faster turnaround times for studies, less manual effort for providers and better patient experience. You can host locally on Amazon S3, Google Cloud, or both. You don't have to be tied to one service provider or platform. PACS users don't have to wait for a specific workstation to be used. The Web-based mode of PACS makes any computer a viewing platform. International standards like DICOM 3.0 are met for communication with medical equipment. The security subsystem is compliant with HIPAA guidelines. The embedded zero footprint viewer is included in the solution and does not require any downloads, installations or plugins.