Best Electronic Data Capture Software for Nonprofit - Page 3

The genuine open-source electronic data capture (EDC) system for clinical research originated from a collaborative effort by volunteers with diverse expertise, including academia, clinical research services, and the IT sector. Today, this initiative is actively utilized by various academic institutions, hospitals, and emerging companies or startups, showcasing its widespread acceptance and adaptability in the field. This collaborative approach has fostered innovation and efficiency in the data collection process for clinical studies.

oomnia is a unified clinical trial system designed to simplify clinical trials regardless of phase or therapeutic area. It brings together EDC, RTSM, CTMS, eTMF, ePRO, and eCOA into one real-time, interoperable SaaS system, ensuring faster execution, full compliance, and clean data across your entire trial.

LabRelations is an innovative and adaptable laboratory platform designed to consolidate and optimize scientific and testing workflows by integrating essential modules like LIMS, ELN, CTMS, and EDC into a cohesive system that facilitates everything from sample tracking and experiment logging to study oversight and compliance reporting. This comprehensive tool not only minimizes manual tasks, inaccuracies, and data fragmentation but also allows laboratories to house all their information in one centralized location. Users can establish rule-based workflows and automations, link instruments and outside systems, as well as ensure complete audit trails and adherence to regulations such as GxP and 21 CFR. Furthermore, LabRelations provides the flexibility to tailor objects, forms, views, and permissions to meet the unique requirements of each lab, thereby enhancing collaboration across various functions and offering real-time insights spanning from research and quality assurance to clinical studies and highly regulated settings. As a result, this platform significantly elevates the efficiency and reliability of laboratory operations.

TrialMaster, the most intuitive Electronic Data Capture (EDC), Suite on the Market, offers superior usability and flexibility. It is your EDC solution for Phase I to IV clinical trials. TrialMaster increases efficiencies and reduces workflow impact, while improving data quality, which results in faster study submissions. TrialMaster's built-in ePro enables site researchers, patients to self-report their outcomes, and sponsor staff access the platform from any device (desktop or tablet, smart phone, tablet, or laptop). All system screens adjust in real-time to the device's size. Single sign-on (SSO), which allows sponsors to use their own IdP to authenticate, reduces the need for multiple passwords and user names.

Medrio's Electronic Data Capture (EDC) platform and complimenting eClinical solutions such as ePRO, RTSM, eConsent, and Direct Data Capture (DDC) have been trusted by major pharmaceutical, biotech, CRO, animal health, medical device, and diagnostic companies since 2005. We are known for our easy-to-use solutions, delivering speed and simplicity to clinical trials of all phases, sizes, and complexities. Medrio users can build their databases in an average of 2.8 weeks with no programming required, make mid-study changes with just a few clicks of a mouse, and much more. From bolt-on capabilities to full-service offerings, Medrio offers flexible, modular solutions that give our customers exactly what they need – and none of what they don’t. Our innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.

Collect remote data safely at any time and from any location using Kordata. This adaptable mobile data collection tool empowers organizations to securely obtain essential information, store it in a centralized cloud system, and distribute it to the appropriate individuals on their devices. In addition, Kordata provides customizable data collection forms and workflows that can be tailored to fulfill unique business requirements, ensuring a seamless data management experience. With its user-friendly interface, Kordata enhances productivity and simplifies the process of data handling for teams across various industries.

Zelta is a cloud-powered platform for unified clinical data management and acquisition, designed to streamline and enhance clinical trial processes. Its modular architecture adapts to the unique demands of each study, enabling faster and more efficient outcomes. With capabilities such as electronic data capture, clinical operations management—including randomization and trial supply tracking—clinical trial management, and electronic trial master file functionality, Zelta supports comprehensive study oversight. It also enhances patient and provider engagement with electronic clinical outcome assessments and e-consent solutions. Built for studies across all phases, therapeutic areas, and global regions, Zelta offers an intuitive user experience with secure single sign-on access from anywhere. Its flexible and scalable design allows for seamless customization and integration with both native and third-party technologies, ensuring adaptability to diverse research needs.

Dokmee Capture Scanning Solution is a document capture platform that allows users to improve business processes without any limitations or per-click charges. Dokmee Capture features offer unlimited scanning, automated data capture, auditing, and reporting tools. Dokmee Capture includes the Magic Index module, which provides users with an easier way to index.

Prelude EDC is a web-based EDC (electronic data capture) solution that helps researchers and clinicians with clinical trial management. Key features include electronic data capture, data management, project management, custom fields, and compliance management. Prelude EDC comes with a drag-and-drop functionality, which helps administrators create electronic case report forms that are configured based on parameters such as entry fields, edit checks, calculations, and more. It allows users to streamline processes for searching, report generation, statistical reporting, and data querying, in order to optimize the preparation of datasets. Plus, the system comes with an in-built library of case report forms for producing reports on metrics such as patient demographics, deviations, adverse events, and study completion rates. Prelude EDC includes an XML export capability, allowing managers to import files into statistical analysis software. Its mobile application enables researchers to collect data and schedule daily, weekly, and monthly surveys.

Introducing an integrated suite of professional tools designed to facilitate dynamic sharing of pre-clinical study data globally, featuring advanced capabilities and widely recognized industry standards. The Seralogix Study Manager™ platform seeks to create a standardized and efficient process for managing pre-clinical studies through a user-friendly interface. It caters to both individual researchers and large-scale research enterprises, harnessing powerful computational resources to simplify experimental design, data collection, and reporting. With this set of tools, you and your team can be assured of high data quality while reaping the advantages of immediate reporting. Successfully planning your experimental design can often feel overwhelming, but Seralogix Study Manager guides you through each step necessary to achieve the statistical rigor required for the success of your studies, ultimately transforming the way research is conducted. As you navigate this innovative platform, you'll discover how it can enhance collaboration and elevate the overall quality of research outcomes.

Our tech-first, always-on document verification protects you and your clients against fraud losses. IDscan uses ISO 30107-3 Level 2, Passive Liveness Detection technology accredited by iBeta to help our customers quickly authenticate the ID documents of their customers. Our ability to layer data on documents gives you the best solution available in the market. Configure the authentication rules so that they automatically accept, reject and refer decisions according to your risk assessment. Software designed for global trading can help you quickly and easily uncover the identities of individuals around the globe and ensure compliance with global regulations.

onPhase is a comprehensive financial automation platform that helps businesses optimize their back-office operations. By automating processes like invoice capture, approvals, and payments, onPhase reduces manual errors and speeds up workflows. The AI-powered system ensures that invoices are processed accurately through intelligent 2-way, 3-way, or 4-way matching, improving financial transparency. It also provides powerful document management capabilities, keeping contracts, W-9s, and receipts secure and audit-ready. The platform integrates with leading ERP systems like NetSuite, SAP, and Microsoft Dynamics, ensuring smooth data flow across various systems and real-time updates, which enhances organizational efficiency. With onPhase, companies can focus more on strategic tasks while automating routine back-office functions.

Flask Data equips life science research and development teams with timely clinical data and solutions for patient safety. The Flaskdata.io cloud API platform streamlines data collection applications for patients, researchers, site coordinators, connected devices, and pharmaceuticals. Our offerings in data management and safety oversight are designed to mitigate risks related to clinical data integrity, patient well-being, and adherence to protocols. The Flaskdata.io platform is not only automated but also scalable and responsive to the specific requirements of your clinical trials. Flask Data is a tech firm that focuses on clinical data oversight and management. We excel in delivering optimal solutions that ensure the highest quality of clinical data while prioritizing patient safety. Recognizing that there is no universal solution applicable to all clinical trials, we dedicate ourselves to thoroughly understanding your distinctive challenges. Collaborating closely with your team, we strive to create tailored solutions that meet your needs for high-quality clinical data and enhanced patient safety, ultimately driving the success of your research initiatives.

Replior is a pioneering company specializing in software solutions for clinical trials, featuring an integrated platform that encompasses EDC, eConsent, ePRO, and Virtual Visits to enhance trial execution. Our comprehensive system, known as Trial Online, facilitates the seamless collection and management of data from investigators, participants, and wearable devices in an efficient manner. It is designed to accommodate decentralized clinical trials (DCT), allowing for flexibility with site visits, remote interactions, or a combination of both. Our journey commenced two decades ago when we were approached to create an online CRF service for a major pharmaceutical firm, marking our transition from an IT operations provider to a dedicated software developer for clinical data collection. Over the years, we have expanded our offerings to include a complete suite of data collection services, while our IT operations are expertly managed by our highly qualified sister company, Complior. As we continue to innovate, our commitment to enhancing clinical trial processes remains at the forefront of our mission.

Marvin is a software platform that provides solutions for Clinical Data Management. This includes EDC (including IWRS/Drug Management and WebPRO), reporting, and more. ), Coding and Composer (CDISC ODM based study design including SDTM map), SDTM visualization, Clinical Document Management, (eTMF), and a mobile app for direct communication between Investigators & patients. Our software and technical support help accelerate clinical trials around the world. Founded in 2002, XClinical is an international eClinical vendor. Marvin, the company's software platform, provides solutions for Clinical Data Management such as EDC (including IWRS/Drug Management and WebPRO), reporting, and more. ), Coding and Composer (CDISC ODM based study design including SDTM map), SDTM visualization, Clinical Document Management, (eTMF), and a mobile app for direct communication between Investigators & patients. Our software and technical support help accelerate clinical trials around the world.

The Registries platform by CSAM, formerly known as MedSciNet Registries, offers a comprehensive and adaptable online space for the management of registries, equipped with robust tools that support every stage of a project's lifecycle, from initial data collection to in-depth analysis. Leveraging a decade of expertise in creating web-based solutions for medical research, CSAM's Registries system presents an advanced application suite designed to host, manage, and oversee registry projects of any scale. This standard system implementation includes all necessary components to establish a fully operational registry, enabling sophisticated data entry forms, customizable workflow configurations, and enhanced data validation, monitoring, and analytical capabilities. Additionally, the platform is designed with user-friendliness in mind, ensuring that researchers can seamlessly navigate through their registry projects while maintaining high data integrity and compliance.

Data MATRIX offers a comprehensive SaaS solution specifically designed for clinical trials. Since its inception in 2009, the Data MATRIX team has specialized in the processing and analysis of clinical data, creating documents that comply with the standards set by the Russian Ministry of Health, FDA, and EMA. Our software streamlines clinical trial processes, allowing users to efficiently manage and track progress online. Before launching a project, we meticulously adjust and validate our software to ensure that every aspect is considered for optimal performance. With a proven track record of completing 180 projects for pharmaceutical companies, biotech firms, and CROs, our solutions have led 6 out of the top 10 Big Pharma companies to achieve a 15% reduction in R&D expenses. Our dedicated team members take pride in their involvement with professional organizations that connect clinical data professionals such as CDISC, ACDM, SCDM, biostatisticians like ISBC, and medical writers associated with EMWA and AMWA. By continually enhancing our offerings, we remain committed to driving innovation in the clinical research landscape.

secuTrial® is a comprehensive, browser-based EDC system that adheres to GCP standards for gathering patient information in both clinical trials and non-interventional research, as well as patient registries. Since its inception in 2000, secuTrial® has been utilized in more than 600 studies and long-term projects globally, undertaken by universities, CROs, medical technology companies, and pharmaceutical organizations, highlighting its exceptional quality, versatility, and high levels of user satisfaction. This robust web-based software solution facilitates the collection and management of patient data for multi-center clinical studies entirely online. It guarantees compliance with all relevant licensing and data privacy laws while maintaining the highest quality benchmarks, ensuring that user needs are met effectively. The continued use of secuTrial® in diverse research settings underscores its reliability and the trust it has garnered in the scientific community.

CIOs, CFOs, COOs, and CCOs, let's collaborate to significantly reduce your time, effort, and expenses by utilizing the most advanced document automation platform available. Eliminate tedious tasks and witness a remarkable boost in employee satisfaction. This comprehensive cloud solution combines capture, RPA, and ECM into a seamless experience. KnowledgeLake effortlessly integrates with your current systems and applications, allowing you to be operational in just days rather than the typical months or quarters. With straightforward configuration and advanced machine learning technology, minimal training is needed. Enhancing customer experience is impossible without first improving employee experience, so empower your workforce with an efficient way to accomplish their tasks, no matter where they are. Our Robotic Process Automation and Artificial Intelligence features alert you to any unusual or noncompliant activities within your systems, all captured in real-time. Furthermore, you don’t need to abandon your legacy systems to keep pace with the evolving landscape of digital business. Discover how we can enable you to operate securely and cost-effectively in this new era. Let us show you the transformative power of modern technology in streamlining your operations.

The integration of eCOA and digital technologies is paving the way for the future of clinical research, seamlessly connecting traditional methods with innovative, patient-centered approaches. Choose YPrime's eCOA solutions to not only obtain high-quality patient data but also to enhance the overall user experience for sponsors, investigator sites, and patients alike. By employing a flexible software development strategy, YPrime is able to swiftly tailor and adapt functionalities to meet specific study requirements within an impressive timeframe of 8 to 12 weeks. Our engaging and visual design process allows clients to review the system at various stages of development, ensuring they are informed before the system goes live. Additionally, our pre-validated and customizable authoring environment not only streamlines startup timelines but also accommodates post-production adjustments, such as changes to study protocols, making it an indispensable asset for clinical research. This commitment to agility and responsiveness positions YPrime as a leader in the evolving landscape of clinical trials.

The BSCAN Standard serves as an independent capture solution or as part of a multi-tiered capture system. It comes in four different capacities: Personal, Low, Medium, and High Volume. One of the standout features of BSCAN is its robust customization options, enabling users to create intricate WorkFlows that include tailored screens, commands, key entry interfaces, and mouse-driven image processing capabilities. Its intuitive controls provide a variety of pre-defined screen layouts that ensure optimal image clarity for quality control, or users can opt to design their own custom layouts that focus solely on the functions they require for maximum efficiency. Setting up either a straightforward single scan and release station or an elaborate WorkFlow system with numerous stations is made easy with BSCAN's Wizard. Users can choose from a collection of sample capture WorkFlow templates or create their own, and the Wizard guides them through each step of the configuration process seamlessly. This level of flexibility and user support makes BSCAN an invaluable tool for any scanning operation, regardless of complexity.

Leveraging our bespoke software development expertise, Ascerteon® has evolved over a span of 15 years through ongoing improvements. The Prestige team is dedicated to creating and managing a diverse array of robust business applications tailored to meet varying requirements. By utilizing cutting-edge web standards and frameworks, Prestige designs sleek and interactive mobile websites that efficiently manage all your data-related needs. Our collaboration with numerous CMS solutions empowers clients to take charge of their own content seamlessly. We offer both onsite and remote assistance for a comprehensive range of IT needs, including backup and disaster recovery, firewalls, mobile devices, networking equipment, servers, and workstations. When it comes to certification operations, don't compromise with software that merely meets the standards; Ascerteon delivers a complete solution, featuring a robust backend for certifying organizational staff paired with an accessible web-based frontend for certificate management. This comprehensive approach ensures that all your certification processes are handled with the utmost efficiency and precision.

Any organization that accepts checks as a payment method can take advantage of AQ2 Remittance. This solution is adaptable for companies that handle a modest volume of 25 to 50 checks each day, scaling up to accommodate hundreds or even thousands of checks on a daily basis. By utilizing advanced check capture technology, businesses can drastically lower their operational and staffing expenses. AQ2 Remittance enables users to swiftly send check images and pertinent information electronically, eliminating the need for couriers or frequent trips to a local bank branch. In addition, the burdensome expenses associated with manually recording check amounts on deposit slips, conducting manual research, and distributing physical copies are effectively eliminated. This comprehensive check capture and electronic deposit service is designed specifically for businesses. With AQ2 Remittance, you can seamlessly capture data for efficient uploading into your accounts receivable system, enhancing overall productivity and accuracy. Ultimately, this innovative solution streamlines financial operations, freeing up valuable resources for other critical business activities.

ActiView is a comprehensive acquisition tool that showcases all ActiveTwo channels on a screen while saving the data in .BDF format to a network disk. The user-friendly layout allows for a swift assessment of data quality. This software is capable of acquiring EEG, ECG, and EMG signals, in addition to data from various external sensors like the AnalogInputBox (AIB), digital triggers sourced from the USB2 receiver, and other devices linked to the AD-box, including respiration monitors, GSR sensors, temperature gauges, ergometers, and plethysmographs. Users can select from multiple reference options, apply filters, and utilize downsampling features. Thanks to our unique single-buffered approach, the acquisition process remains stable and dependable even during multitasking, as the DMA transfer to a large intermediate ring buffer guarantees that no data is lost. ActiView is an open-source program developed in LabVIEW, making it an exceptionally flexible resource for researchers who wish to modify and enhance the software to suit their specific needs. Its adaptability and robust features position it as an invaluable asset in experimental setups.

The AcqKnowledge Demo software provides an efficient simulation of physiological data recording across multiple systems and transducers, while also encompassing a wide range of comprehensive features. It includes a collection of sample data files showcasing recordings made with equipment from MP Research Systems, BioHarness, Mobita, B-Alert, Epoch, and Stellar, featuring both human and animal subjects. This demo serves to illustrate the key functionalities of the AcqKnowledge software, utilizing the provided sample data files for demonstration. Users can explore specific components, gather measurements, and conduct analyses, making it a valuable tool for educational purposes. The user-friendly Startup Wizard interface of the AcqKnowledge Demo allows for easy access to sample data files and pre-configured graph templates, enhancing the overall experience. This software is an excellent resource for those interested in understanding physiological data analysis in a practical context.