Top ActiView Alternatives

OpenClinica stands out as a prominent provider of software solutions for managing clinical data. Their robust tools are designed to enhance the compliance and efficiency of clinical trials. The main offerings from OpenClinica include OpenClinica Enterprise, OpenClinica Participate, and OpenClinica Randomize, which together facilitate a comprehensive approach to clinical data management. Each product addresses specific needs within the clinical research landscape, making them essential for successful trial execution. OpenClinica is an industry-leading platform that enables more efficient and effective clinical trials by providing a comprehensive range of tools for managing data, patient engagement, and recruitment. Key features include electronic data capture (EDC), patient-reported outcomes (ePRO), and fully automated eConsent, all designed to improve accuracy and streamline study workflows. The platform supports EHR-to-EDC integration, reducing manual errors and accelerating data collection. OpenClinica also offers robust reporting and data analysis tools, ensuring real-time insights into trial progress. With over 15,000 studies powered and more than three million patients involved, OpenClinica is trusted by life sciences organizations worldwide, from pharmaceutical companies to academic researchers and government bodies. Its seamless integration, user-friendly design, and comprehensive features make it an essential tool for advancing clinical research.

Castor is an innovative clinical trial platform designed to simplify data management through electronic data capture (EDC), eConsent, and patient-reported outcomes (ePRO). Its flexible and user-friendly interface allows researchers to collect, manage, and analyze clinical data efficiently across multiple sites and remote patients. Castor’s tools are specifically designed to support decentralized clinical trials (DCTs), enabling real-time data monitoring, remote recruitment, and seamless patient engagement. The platform ensures full regulatory compliance, including HIPAA, GDPR, and 21 CFR Part 11, and is certified for ISO standards. With more than 50,000 global users, Castor continues to improve the speed and quality of clinical trials through integrated, scalable solutions that reduce administrative burdens and accelerate research.

Advanced eClinical Solutions for EDC/ERT/eCOA markedly accelerates the initiation and conclusion of clinical trials by as much as five days, slashes costs related to monitoring by nearly 80%, and enhances both capitalization and appeal, with 89% of clients acknowledging its benefits. A remarkable 96% of data science professionals affirm that it fosters growth and innovation within the fields of Data Management and Data Science. Furthermore, 94% of researchers appreciate the user-friendly nature of the interfaces. Additionally, a robust internal expertise in Data Management 365 is a crucial component of our Data Management 365 strategy, enabling us to not only gain deeper insights into the hurdles encountered by Data Managers but also to refine MainEDC™ and share valuable technology and best practices with our clients effectively. This commitment to excellence ensures that we remain at the forefront of the industry while supporting our clients' success.

Transforming documents, email data, and databases into actionable insights is made seamless with PSIcapture, which serves as more than just a basic tool for converting paper documents into digital formats. This sophisticated, automated document capture system excels at extracting data from physical documents and transforming it into a digital medium. It is designed to fulfill the diverse needs of any organization, accommodating the ever-evolving landscape of document management software and scanning technologies. PSIcapture stands out with its exceptional capability to integrate with a wide range of scanners and seamlessly route data to over 60 enterprise content management systems. Regardless of the size of the organization, PSIcapture simplifies and enhances the document processing experience. This versatile document capture platform is not only cost-effective and scalable but also uniquely adaptable to meet the specific requirements of every organization. By consolidating all document management needs into a single capture platform, PSIcapture ensures efficiency and effectiveness across various operational frameworks. In a world where information flows constantly, having a reliable system like PSIcapture can significantly streamline workflows and improve productivity.

Zelta serves as a cloud-based platform dedicated to the unified management and acquisition of clinical data, aiming to optimize and improve the processes involved in clinical trials. Its flexible modular structure is tailored to meet the specific requirements of different studies, which leads to quicker and more effective results. With features that include electronic data capture, management of clinical operations—such as randomization and tracking of trial supplies—clinical trial oversight, and electronic trial master file capabilities, Zelta provides thorough supervision of studies. Additionally, it fosters engagement among patients and providers through electronic clinical outcome assessments and e-consent options. Suitable for a range of studies across all phases, therapeutic disciplines, and international locations, Zelta is designed to offer a user-friendly experience with secure single sign-on access available from any location. Its adaptable and scalable framework permits easy customization and seamless integration with both proprietary and third-party technologies, ensuring it can meet various research requirements effectively. This makes Zelta an invaluable tool for researchers looking to streamline their clinical trial efforts.

Reduce the time spent on daily manual tasks to focus on delivering exceptional services. Thread’s ABA data collection tool equips clinical teams with the necessary resources to provide high-quality care for clients, manage programs effectively, and streamline data collection and ABA graphing in a unified platform. This mobile-friendly solution supports direct care teams in tackling the challenges of client care while on the move, facilitating a more manageable workflow. With the ability to quickly access client data sheets for both online and offline data collection, teams can efficiently monitor intervals, percent correct, duration, task analysis, and generate real-time graphs and reports, thereby improving the standard of clinical care offered. Crafted for simplicity, Thread’s user-friendly application allows ABA practices and clinical teams to begin implementation within just an hour, enabling them to focus on what truly counts—success in their practice while delivering top-notch care. This increased efficiency not only frees up time for team members to interact with clients on a more personal level but also fosters a deeper connection, further elevating the overall service quality provided. By minimizing administrative burdens, your teams can concentrate on building relationships and delivering customized support to each client.

DiData is a versatile web-based software platform that can be tailored to fulfill various client requirements. It offers three primary functionalities: - Laboratory stock management through Di-Freeze - An Electronic Data Capture System known as Di-EDC - A comprehensive Laboratory Information Management System referred to as Di-Lims. Among its standout characteristics are rapid data rendering capabilities and exceptional usability when handling large datasets, along with swift deployment options that allow seamless integration with existing systems and instruments via available libraries and a REST API. Users can enhance their data analysis with features such as filters, editable columns, and highlight options for optimal data visualization. Additionally, the customizable dashboard module can be adjusted to align with specific user needs. For further information, our website provides an extensive overview of additional features and advantages offered by DiData.

Prism is a versatile statistical software developed specifically for scientists, as opposed to statisticians. You can begin your analysis by entering data into specially designed tables for scientific research, which will guide you in choosing statistical techniques that improve your research productivity without requiring any programming skills. Throughout this journey, you will receive valuable insights and support, enabling you to make well-informed choices regarding your analyses, understand the critical assumptions at play, and accurately interpret your results. Moreover, Prism simplifies collaboration with colleagues, making it easy to obtain feedback from peers and disseminate your research findings to a broader audience with minimal effort. The transition from raw data to polished, publication-ready graphs is seamless and straightforward. Prism also offers a plethora of customization options for your visual outputs, including different color schemes and methods for organizing data. You have the flexibility to export your work in various formats, share it directly to PowerPoint, or even email it straight from the application. In addition, you can bolster your expertise in data analysis and visualization through exclusive educational materials designed by experienced professionals in the field, ensuring you are equipped to tackle any research challenge effectively. With its intuitive interface and comprehensive features, Prism not only streamlines the research process but also empowers users to meet and exceed their research objectives. This combination of functionality and user support makes Prism an invaluable tool for scientists at every level.

The Net Station 5.4 software suite from EGI offers a comprehensive platform that integrates EEG, electrical source imaging, and neuromodulation, providing laboratories with the tools they need to innovate and grow. This software is distinguished by its impressive speed and performance, which allow for quick data processing, and it includes a user-friendly dashboard that facilitates efficient data review and analysis, making it easier for users to learn and train. Furthermore, it is designed for scalability, accommodating the addition of features for source imaging and neuromodulation, while also ensuring seamless compatibility with various external hardware and software. A significant enhancement is the inclusion of the EEGLAB plug-in, which broadens interoperability with the GES High-Density EEG System and represents an important move towards providing open-source resources that expand access to high-density EEG research. The Net Station 5.4 Acquisition feature significantly streamlines EEG data collection, enabling users to effortlessly choose montages, set up filters, check impedances, and insert events directly from the main interface, thereby optimizing the entire data acquisition process. This forward-thinking design not only enhances overall productivity but also equips researchers with the capability to analyze and interpret their findings with greater efficacy. Ultimately, EGI's commitment to continuous improvement ensures that users are always at the forefront of EEG technology advancements.

CSAM's Registries platform, which was previously recognized as MedSciNet Registries, provides a versatile and extensive online environment for registry management, featuring powerful tools that facilitate each phase of a project's lifecycle, from the initial stages of data collection to comprehensive analytical processes. Drawing upon a decade of experience in developing web solutions tailored for medical research, the Registries system from CSAM offers a sophisticated application suite capable of hosting, managing, and supervising registry initiatives of any magnitude. This standardized implementation encompasses all essential elements required to set up a fully functional registry, thus allowing for advanced data entry forms, tailored workflow setups, and improved data validation, oversight, and analysis capabilities. Furthermore, the platform is crafted with user friendliness as a priority, making it easier for researchers to navigate their registry projects effectively while ensuring the preservation of high data integrity and adherence to compliance standards. The intuitive design of the interface helps streamline the research process, ultimately enhancing productivity and efficiency for users engaged in complex registry projects.

Medidata's Rave EDC (Electronic Data Capture) is recognized as the leading system for effectively handling clinical trial data from various sources like sites, patients, and laboratories, ensuring both sophistication and security. As a key component of the Medidata Clinical Cloud™, it provides an all-encompassing platform that harmonizes multiple processes, thus removing the need for data reconciliation and enabling thorough data analysis across various studies and functions. Users are able to manage their responsibilities, studies, and sites through a unified dashboard that integrates all Rave EDC and other Medidata Clinical Cloud tools. This platform significantly reduces the risks of duplicate study master data and discrepancies, such as inconsistent IDs for identical sites across different applications. Central to Medidata’s unified strategy for Clinical Data Capture and Management, Rave EDC supports the smooth collection and reconciliation of data from an array of sources, including Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging, and Sensor Cloud; it also bolsters data review and analysis with sophisticated tools like Rave TSDV and Medidata Detect. By offering these advanced functionalities, Rave EDC not only streamlines the data management process but also empowers clinical researchers to make well-informed decisions grounded in trustworthy and comprehensive data insights. Therefore, it plays an essential role in enhancing the overall efficiency and effectiveness of clinical trials.

BLU DELTA is a cutting-edge invoice capture tool that employs genuine AI technology to convert digital receipts into efficient automation systems. Engineered for professionalism, speed, and user-friendliness, it drastically cuts down on processing times and reduces acquisition costs without requiring any setup or training. Users will notice instant enhancements in recognition accuracy, making it a compelling choice for businesses. The platform is adaptable, offering both cloud and on-site deployment options, along with integration capabilities via API or web interface. With its advanced AI features that surpass simple OCR, businesses can transform their digitization processes into significant assets. Notably, it boasts impressive recognition rates of up to 99%, even handling unusual invoice formats, thereby facilitating optimal automation for employees and alleviating them from repetitive tasks. The straightforward licensing model and easy setup further diminish costs, allowing organizations to quickly realize a return on their investment. Regular updates and support are included, ensuring that users benefit from continuous enhancements without incurring additional charges. The BLU DELTA Capture Service can be accessed through either Microsoft Azure's cloud infrastructure or an on-premise solution, ensuring that company data remains fully protected regardless of the selected method. This inventive strategy not only enhances operational workflows but also plays a crucial role in boosting overall business productivity and effectiveness. Thus, BLU DELTA stands out as a transformative solution in the realm of invoice processing.

Effective data management plays a vital role in enhancing the success and overall efficiency of clinical research endeavors. Although the process can be intricate, Quanta View, an electronic case report form (e-CRF), facilitates streamlined data processing control. This platform incorporates features like real-time monitoring, tracking of participant inclusions, and comprehensive project management. Quanta View is designed to support you in every facet of your clinical research journey. It is easily accessible online and features a responsive design that adjusts seamlessly to various devices, including tablets and laptops. Tailored specifically for the pharmaceutical, medical device, and cosmetic sectors, Quanta View ensures that all research needs are met with precision and adaptability. It is an essential tool for researchers aiming to optimize their workflows and enhance data integrity.

The Ecobot wetland mapping application stands out as the sole software capable of delivering unparalleled efficiency and precision for wetland scientists at AEC, catering to a diverse range of users including counties, state and federal Departments of Transportation, mitigation banking entities, utility and oil and gas companies, as well as firms specializing in natural resource consulting. This innovative tool is accessible through the Apple App Store for both iPhone and iPad and proudly operates as an Esri Startup partner. By utilizing Ecobot, users can significantly reduce their project time by 50%, eliminating the need for reference guides and providing instant, accurate USACE PDF outputs. Its user-friendly interface requires no additional training, making it easy to adopt. Having successfully facilitated the submission of over 7,500 USACE wetland determination forms, Ecobot has proven to be an invaluable asset, decreasing overall workloads and saving AEC and environmental consulting firms more than 4,500 hours of effort. This remarkable efficiency redefines productivity in wetland management and sets a new standard for the industry.

FormFoundry is an adaptable online platform that enables organizations to develop custom data collection applications tailored to their unique needs. With its state-of-the-art web form builder, users can easily create native mobile applications for field personnel, while its flexible data platform offers a holistic view of critical business functions. Designed to resolve issues in data management, FormFoundry significantly streamlines the data collection process. Empower your organization with robust form creation capabilities, personalized asset management, and intricate workflow setups, all customized to fit your exact specifications. The consequences of ineffective data management, such as mislabeling files and data corruption, can pose serious obstacles for any business. Furthermore, the slow pace of manual data entry and review can hinder some companies from keeping up with the swiftly changing digital landscape, underscoring the need for contemporary solutions. By implementing FormFoundry, organizations can overcome these challenges and maintain their edge in today’s dynamic environment. This powerful platform not only enhances efficiency but also fosters innovation in data handling.

Effortlessly manage your clinical trial data with sophistication using Clincase’s innovative e-Clinical Technology Solutions. This comprehensive platform offers a wide range of features, services, and additional functionalities that can be accessed with a single login. Its robust and adaptable EDC software keeps data managers, monitors, and sponsors connected to the progress and performance of the study, while simultaneously encouraging increased engagement from sites and investigators. Clincase prioritizes user-friendly and effective solutions that allow for real-time access to data. As a zero-footprint solution, it employs secure and encrypted data transfers to ensure safety. The clinical trial information is securely hosted in Germany, adhering to the highest standards of physical security. Our architecture is designed for redundancy, ensuring that data is consistently mirrored to a secondary data center for enhanced reliability, complemented by daily full backups to maintain data integrity and availability. By choosing Clincase, you can optimize the clinical trial process while fostering improved collaboration among all stakeholders involved, ultimately leading to more successful outcomes. Additionally, our commitment to innovation means that we continuously update our solutions to meet the evolving needs of the industry.

When a job opening is announced, it prompts a surge of resumes to arrive through multiple avenues, including mail, email, and fax, each varying in format and requiring meticulous review to pinpoint the ideal candidate. The need for swift results is paramount, as your company is vying for a contract that demands individuals with precise skills and expertise, which limits the time available to craft the required proposal while also evaluating the skills of your current team. In this context, the Generic Resume Data Management System created by Working Solutions International stands out as an essential tool. This system features a standardized Generic Resume form that can be shared with applicants by employers and recruiters, alongside a reporting tool that efficiently compiles, organizes, and presents the gathered information. In contrast to conventional resumes sent via paper, fax, or email, Generic Resumes are organized in real-time and are easily searchable, which significantly cuts down the duration that employers need for candidate evaluations. By simplifying the resume assessment process, the system not only boosts productivity but also paves the way for more informed hiring choices. Ultimately, this innovative approach to resume management ensures that companies can swiftly navigate the competitive hiring landscape while making choices that best serve their needs.

At Calyx, we recognize that the success of any clinical development project hinges on the integrity of your data, highlighting the crucial role of an effective electronic data collection (EDC) system. Utilized in more than 2,600 clinical trials around the world, Calyx EDC streamlines the collection and reporting of clinical trial data through a platform that is both intuitive and efficient. It is vital to protect your essential data with a dependable partner—contact us to learn how Calyx can bolster the success of your initiative. With Calyx EDC, you acquire the flexibility to seamlessly plan, design, and manage studies, regardless of their complexity. Its comprehensive features are designed to reduce costs, improve site visibility, and enhance overall efficiency, ensuring your trial stays on track. Count on Calyx to be the support you need to navigate the intricate landscape of clinical trials, enabling you to focus on what truly matters. Your journey toward successful clinical outcomes begins with the right partnership.

Our innovative, always-active document verification system safeguards both you and your clients from potential fraud losses. Utilizing ISO 30107-3 Level 2 Passive Liveness Detection technology certified by iBeta, IDscan enables rapid authentication of customer ID documents. The unique capability to layer data on documents provides you with the most effective solution available today. You can set up authentication rules to automatically accept, reject, or refer decisions based on your specific risk evaluation. Furthermore, software tailored for international trade allows you to efficiently identify individuals worldwide while ensuring adherence to global regulatory standards. This comprehensive approach not only enhances security but also streamlines the verification process across various jurisdictions.

Discover exceptional insights with unmatched flexibility and versatility through LabChart, a physiological data analysis software that effortlessly integrates all your recording devices, allowing for the concurrent collection of biological signals from various sources while performing complex calculations and visualizations in real time during experimental procedures. Instantly assess metrics like Mean Arterial Pressure, Systolic Pressure, and Max dP/dt from blood pressure recordings within moments. The Blood Pressure module is not only user-friendly but also provides quick results, and our intuitive two-point calibration tool makes the conversion of voltage units to standard measurement units a breeze. LabChart is engineered to execute fundamental tasks with ease, keeping advanced features discreet until required. You can customize LabChart to suit your needs by employing scripting and automation options available on Windows, and take advantage of custom arithmetic, alongside import and export functionalities across numerous formats for seamless integration with other software solutions. Elevate your physiological data analysis to unprecedented levels of efficiency and accuracy with LabChart, ensuring that your research reaches its full potential seamlessly.

WizzForms Desktop streamlines the process of filling out various forms by allowing users to scan IDs such as driver's licenses, state identification cards, or passports to automatically fill in information. This software can be seamlessly incorporated into a wide range of applications, including point-of-sale systems and visitor management platforms. Its user-friendly integration capabilities make it suitable for any existing software, facilitating efficient data capture and auto-population. With WizzForms, users can swiftly scan any government-issued ID, including military identification and permits, to transfer the relevant details into digital forms. Furthermore, it is compatible with all Windows applications, encompassing text-entry programs like MS Excel and Google Docs, as well as web-based tools, making it an ideal solution for diverse data entry needs. Setting up WizzForms is a straightforward process, ensuring that users can quickly benefit from its functionality. By simplifying form completion, WizzForms significantly enhances productivity and accuracy in data handling.

In comparison to other Electronic Data Capture (EDC) systems offered by firms like MediData, DataTrack, and Omnicomm, TrialStat emerges as the most all-encompassing suite of tools for study management, providing seamless integration with a variety of external data sources such as electronic medical records (EMR), wearable technology, and both clinical and non-clinical information systems. TrialStat offers a unified platform that supports every stage and type of clinical trial. Our EDC suite is equipped with a single sign-on feature and accommodates multiple tenants, featuring modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, a Vendor Neutral Imaging Archive, a comprehensive Reporting and Analytics Portal, and customized Machine Learning solutions. With a strong focus on data analysis, TrialStat ensures real-time reporting, on-demand data extracts, and analytics that encompass a single study, a program, or the full breadth of your research portfolio, providing all stakeholders with relevant, tailored, and timely insights into all aspects of study data while identifying potential risks or delays. Furthermore, the platform’s robust integration capabilities enhance collaboration among research teams, resulting in a more streamlined and productive trial management process. This ultimately empowers researchers to make informed decisions that drive the success of their clinical trials.

Gather remote data securely whenever and wherever you need it with Kordata. This versatile mobile data collection solution enables organizations to safely acquire vital information, consolidate it within a centralized cloud system, and share it with the right individuals on their devices. Moreover, Kordata offers customizable data collection forms and workflows that can be adjusted to meet specific business needs, promoting an efficient data management process. Its intuitive interface not only boosts productivity but also streamlines data handling for teams in diverse sectors. Ultimately, Kordata stands out as an essential tool for organizations looking to optimize their data collection and management practices.

Our platform provides a web-based interface specifically crafted for the efficient gathering of data across diverse studies and clinical environments. With its customizable and user-friendly data entry options, it can be adapted to fit any medical specialty, patient group, or research project. The system significantly improves care quality by tracking patient-reported outcomes and utilizing population analytics to inform decisions. Its secure, web-based format guarantees compatibility with both laptops and tablets, ensuring smooth data input regardless of the device used. Researchers enjoy the advantage of real-time reporting features, which allow them to manage the entire study process for both single-site and multi-site trials, regardless of their location. The DADOS Platform boasts a remarkable user interface (UI) and intuitive tools that enable clinicians and researchers to create programs or studies that effectively bridge the gap between research and clinical application. Patients are drawn to DADOS for its ease of use and the ability to access it from virtually anywhere, making it an essential tool in contemporary healthcare settings. Ultimately, this forward-thinking platform nurtures a collaborative atmosphere where research initiatives and patient care can flourish in unison, enhancing the overall quality of healthcare delivery.

Entrypoint is a comprehensive platform designed for the development, deployment, and management of customized data entry applications, allowing users to access data entry and system administration capabilities from virtually anywhere. This collection of user-friendly tools enables individuals to create, execute, and manage a wide variety of bespoke data entry applications, featuring built-in validation, editing functionalities, and various export options. With a plethora of integrated features, Entrypoint facilitates the incorporation of sophisticated elements such as range checks and table lookups, enhancing the overall user experience. The conventional practice of collecting information through paper forms followed by manually inputting it into a digital system is not only labor-intensive but also susceptible to errors in transcription. By adopting electronic forms for direct data entry into a database, organizations can effectively eliminate the cumbersome intermediary paper process and its associated pitfalls. Additionally, the shift to electronic data capture proves increasingly beneficial for organizations confronting higher data volumes and rising costs, as it promotes streamlined processes and improved efficiency in data management. Therefore, Entrypoint emerges as a vital resource for organizations aiming to upgrade and modernize their data processing methodologies, positioning them for greater success in a digital landscape.

GoResearch™ is a sophisticated and rigorously tested online platform crafted by 2KMM for electronic data capture (EDC), tailored specifically for various research projects such as clinical trials, observational studies, and patient registries. It offers an extensive range of features that streamline these projects across different areas, including the ability to customize data workflows and manage procedures related to Adverse Events, complete with automated email notifications to safety teams. Moreover, the platform integrates a randomization module that allows for the random assignment of participants to treatment groups, while also enabling data collection through custom electronic case report forms (eCRF) that cater to the unique requirements of each study. In addition, GoResearch™ supports the incorporation of ePRO, eSource, and mHealth data through dedicated mobile and web applications, and features a flexible application programming interface (API). The aim of this platform is to significantly improve the efficiency and precision of data management in various research environments, ultimately contributing to more reliable outcomes in studies. By providing these robust tools, GoResearch™ empowers researchers to focus on their core objectives while ensuring that data integrity and compliance are maintained throughout the research process.

The analysis of medical imagery powered by artificial intelligence is enhanced through advanced automation of clinical data workflows. Available as either a web-based SaaS or an on-premise solution, UNITY has gained international credibility from top medical technology companies and healthcare organizations for its proficiency in collecting thorough, reliable, and compliant data. Its integrated features for Patient-Reported Outcome Measures (PROM), electronic Case Report Forms (eCRF), and medical image analysis streamline critical data gathering activities, which in turn accelerates and reduces the costs of clinical trials. RAYLYTIC's Imaging Core Lab brings years of expertise to the automated and independent evaluation of musculoskeletal structures and device performance, particularly in the spine, hip, and knee, offering clients exceptional analytical and operational support. This state-of-the-art capability guarantees that healthcare professionals can depend on high-quality data for their decision-making, ultimately enhancing patient outcomes and fostering greater trust in medical processes. By implementing these innovative solutions, healthcare systems can greatly improve efficiency and accuracy in clinical trials.

Fielda enhances the management and inspection of assets, allowing users to work more effectively and without errors. By combining mobile data collection, GIS features, automated processes, and detailed reporting, we simplify field operations significantly. This intuitive mobile data collection solution is specifically designed for organizations that depend on effective data management and collection. With Fielda, your team can conveniently gather asset details, capture images, use GIS mapping, and implement workflows while on-site. As a no-code solution, it enables any team member to easily design an unlimited array of forms or checklists, manage workflows, and share data with team members in real time. You have the ability to customize your workflows, forms, priorities, and reports to meet your unique requirements. Furthermore, you can oversee projects efficiently by making decisions based on up-to-date insights, empowering supervisors and managers to effectively manage and coordinate several projects at once. The adaptability and customization features provided by Fielda ensure your team can respond effortlessly to a variety of operational challenges. This level of flexibility not only enhances productivity but also fosters a collaborative environment where team members can contribute more effectively.

Boost the precision and effectiveness of your field data gathering using the INKWRX platform. Effortlessly transition your existing business forms, allowing your team to complete paperwork efficiently with our adaptable data collection solutions, which are compatible with mobile phones, tablets, or digital pens. Explore the extensive features of our Data Collection App. Leverage our intuitive online form builder that employs a drag-and-drop interface, making it simple to develop mobile data collection forms. Quickly gather information across a variety of devices and tools, including smartphones, tablets, or digital pens. Effectively oversee access, users, groups, and workflows. Seamlessly integrate the collected data into your current applications, services, and processes. We have streamlined the form creation process to ensure that anyone familiar with Microsoft Office will find it straightforward to design, style, and launch new forms. You have the option to choose from graphical or converted data elements when building your forms, and you can even combine both formats within a single form. This versatility allows for tailored solutions that cater specifically to your individual data collection requirements. Furthermore, our platform ensures that you can adapt your forms according to changing business needs, maintaining efficiency and relevance over time.

Managing and collecting data can often seem daunting, whether for personal research, complex development portfolios, or extensive development initiatives. Over the span of more than twenty years, Clario has been addressing and overcoming EDC challenges, gaining invaluable insights along the way that we are keen to share. A significant finding is that some clients choose to develop their own EDC solutions to avoid hefty initial costs or long-term commitments. In contrast, others seek a more comprehensive solution that provides a wide range of features and enhanced service, alleviating daily operational worries. Clario’s suite of EDC solutions is delivered through a singular, flexible, and powerful platform, ensuring that all client requirements are effectively fulfilled. Our dedication to innovation and exceptional customer service propels us onward in this ever-changing environment, allowing us to adapt to new challenges efficiently. This commitment not only enriches our offerings but also strengthens our client relationships.

Collect diverse types of form data, including calculations accompanied by checks to ensure accuracy and completeness. Securely capture electronic signatures on your device or online, guaranteeing their digital verification. You can document with photographs or upload images directly from your library, allowing for annotation and integration into sketches. Enhance your documents and images with additional drawings, graphics, and notes to achieve a more refined appearance. naturalForms effortlessly connects with various applications, optimizing your workflow and boosting productivity. Input data with ease through features such as virtual keyboards, checkboxes, dropdown menus, radio buttons, and date and time selectors. It is also possible to designate mandatory fields or implement validation checks to ensure that the information you gather is precise and comprehensive, thereby improving the quality of your forms. This holistic approach not only streamlines the process but also promotes greater efficiency in data collection, making it an invaluable tool for any organization. By leveraging these capabilities, users can significantly reduce errors and enhance their overall operational effectiveness.

Protocol First not only bridges various locations and eliminates obstacles in Clinical Research during the pandemic, but its services continue to hold significant value during normal circumstances as well. What was previously considered optional technology has now transitioned into a necessity. Our solutions promote continuous communication, allowing research not only to survive but to flourish and advance rapidly. With a comprehensive remote monitoring tool that features automatic tagging, our platform integrates effortlessly with any Electronic Data Capture (EDC) system, accessible at any time and from any location. Protocol First emphasizes the importance of connecting Sites, Sponsors, CROs, and different functional areas to foster a unified research environment. We deliver comprehensive solutions that address the myriad challenges encountered in Clinical Research. At the core of Protocol First is a commitment to ensuring the accuracy and proper organization of your data, which increasingly utilizes AI, NLP, and ML technologies. A vital aspect of effectively harnessing AI is the establishment of a solid framework for your data. The software suite provided by Protocol First ensures that information flows seamlessly from patients to the FDA, maximizing the capabilities of data science while enhancing the overall research experience. As we progress, our dedication to innovation will not only persist but also further expand, significantly increasing our influence within the industry. Furthermore, we are committed to adapting our services to meet the evolving demands of the research landscape.

Digitalis is an innovative solution for the collection and management of clinical data, operating as an Electronic Data Capture system. This platform offers all the necessary tools for effective and thorough data management, guaranteeing an enjoyable user experience. Its adaptable and user-centric design emphasizes the software’s ease of use and versatility, customized to satisfy unique user needs. As a web-based application, Digitalis eliminates the need for complex installations; access is granted with just a web browser and a reliable internet connection. It is optimized for contemporary web browsers such as Chrome, Firefox, and Safari, while still maintaining functionality on older versions like Internet Explorer 9. Whether used on a desktop or a tablet, Digitalis ensures a consistent user experience, automatically adjusting to fit any screen size. This careful consideration allows for convenient data collection from mobile devices, making it easy to gather information wherever you may be. Overall, Digitalis significantly improves the management and collection of clinical data, establishing itself as an essential resource in contemporary research environments. The platform not only enhances efficiency but also supports researchers in making informed decisions based on accurate data.

Our customizable forms can be adapted to fit your specific needs, processes, and desired outcomes. Designed to be intuitive and accessible, they cater to teams of all sizes. In just a matter of minutes, you can transform your conventional paper forms into attractive digital documents, boosting your productivity while reducing costs. There's no requirement for extensive training sessions! Culverdocs offers simple and effective data entry solutions that support users throughout the entire procedure. With immediate delivery, you can say goodbye to the delays of paper forms and focus on what truly counts. Additionally, you have the capability to create and share high-quality reports that are aesthetically tailored to showcase your brand, as well as utilize custom dashboards for on-the-fly data reporting and analysis. Our streamlined workflows guarantee that information reaches the right departments effortlessly. Furthermore, incorporating Culverdocs into your existing systems is remarkably straightforward. Our integration capabilities allow you to connect with a range of services or construct a unique integration using any REST service, making adaptability a core attribute of our platform. This level of flexibility not only enhances your organization's ability to react quickly to changing demands but also promotes more effective data utilization, ultimately driving success. Moreover, our ongoing support ensures that you can continually optimize your workflows and harness the full potential of your data.

Encapsia is at the forefront of modern healthcare solutions, transforming the landscape of clinical trials with an exceptionally adaptable and effective system. Developed in the era of smartphones, Encapsia harnesses contemporary innovations to enhance the clinical trial process significantly. Its eSource platform facilitates direct data capture (DDC) while also supporting medical coding, integrating third-party data loads, and offering unparalleled data visualizations. This cutting-edge system stands out as one of the most powerful and inventive tools available for the collection and management of clinical trial data. With real-time data accessibility, users can instantly view all information once entered, enabling proactive oversight of trial advancements and empowering informed decision-making for better management outcomes. Encapsia’s commitment to innovation ensures it remains an essential asset in today’s clinical research environment.

Formic's adaptable technology enables the swift and scalable gathering of multichannel patient experience surveys, assisting over 200 NHS and public sector clients in turning patient feedback into actionable insights, supporting GP revalidation, and establishing a foundation for both immediate and long-term improvements in quality and service. Our patient experience software is versatile, available for onsite deployment, hosting, or as a fully managed solution, ensuring that data is validated at the point of entry and delivering quick, precise, and trustworthy results across paper and digital formats. By accommodating a range of formats, including paper, online platforms, tablets, kiosks, and touchscreens, Formic is engineered to synchronize surveys across various channels, guaranteeing that feedback from multiple organizations is consistent and compiled into a centralized database, which simplifies the analysis process for care providers across different health and care settings. This thorough methodology not only boosts the precision of data collection but also greatly enhances reporting efficiency for healthcare professionals, ultimately contributing to better patient care outcomes. By streamlining these processes, Formic supports healthcare providers in making informed decisions that directly impact service quality and patient satisfaction.

With over 15 years of dedicated experience in custom software development, Ascerteon® has continually refined its services to meet the evolving demands of the industry. The Prestige team is committed to crafting and maintaining a wide variety of robust business applications, specifically designed to address diverse client needs. Utilizing the latest web standards and frameworks, Prestige excels at designing appealing and functional mobile websites that fulfill all data requirements. We work in conjunction with numerous content management systems, enabling our clients to take charge of their own content seamlessly. Our comprehensive support services, available both onsite and remotely, cater to a wide spectrum of IT necessities, including backup and disaster recovery, firewalls, mobile devices, networking hardware, servers, workstations, and much more. It is critical for your certification processes to utilize software that goes beyond just the basic requirements. Ascerteon offers a comprehensive solution, featuring a powerful backend for managing certification activities, paired with a user-friendly web-based frontend tailored for efficient certificate management. By choosing Ascerteon, you can guarantee that your organization not only operates smoothly but also maintains a competitive edge in the marketplace. Furthermore, our commitment to continuous improvement ensures that we adapt and innovate in response to both client feedback and industry trends.

Transforming your field inspections into a digital format is a breeze with Smartflow. This platform allows you to digitize various aspects such as inspections, daily operations, routine checks, checklists, and much more. With Smartflow's intuitive drag-and-drop feature, you can design intricate workflows that give you complete oversight and customization to align with your business challenges and objectives. Additionally, you can seamlessly integrate data from various sources or systems while developing your workflows. Smartflow also delivers real-time analytics and comprehensive data reports that can be shared effortlessly with your clients, enhancing transparency and communication. By leveraging these features, you can significantly boost your operational efficiency and foster stronger client relationships.

The BSCAN Standard is designed to function either as a standalone capture system or as an integral component of a multi-stage capture configuration, offering four unique capacities: Personal, Low, Medium, and High Volume. A key advantage of the BSCAN is its remarkable customization capabilities, enabling users to establish complex workflows through personalized screens, commands, and data entry windows, complemented by mouse-driven image processing options. Additionally, users have access to a selection of pre-configured screen layouts that maximize image clarity for straightforward quality control, while still enjoying the flexibility to develop their own custom interfaces that focus solely on the features they consider essential for streamlined operations. The BSCAN's user-friendly Wizard simplifies the configuration of both basic single scan and release stations and more elaborate workflows involving multiple stations, making the setup process accessible. Users can opt for various sample workflow templates or craft numerous personalized solutions, with the Wizard assisting them in a thorough step-by-step setup process to guarantee peak performance. This level of flexibility and ease of use positions BSCAN as the perfect solution for organizations of any scale aiming to optimize their capture workflows, ultimately leading to enhanced operational efficiency and productivity.

Converting business documents into actionable value is critical for contemporary companies. ABBYY FlexiCapture addresses this need by removing barriers in workflows laden with documents, establishing itself as an Intelligent Document Processing platform tailored for the complexities of the modern digital environment. This cutting-edge solution combines advanced natural language processing, machine learning, and high-level recognition technologies into a unified platform capable of handling a diverse array of document types, from simple forms to complex free-form documents, and is adept at managing everything from single documents to large-scale batch operations under strict service level agreements. By overseeing the complete pathway from document intake to final output, FlexiCapture enhances content-driven business applications such as Robotic Process Automation (RPA) and Business Process Management (BPM), allowing organizations to focus on improving customer service, minimizing costs, maintaining compliance, and securing a competitive advantage. Consequently, a growing number of businesses are realizing significant cost savings by utilizing Intelligent Process Automation to identify and seize automation opportunities, thereby refining their operations for greater efficiency and speed. This transformation not only simplifies workflows but also empowers organizations to better utilize their resources, paving the way for innovation and sustainable growth, ultimately enhancing their overall market position.

Effective management of clinical data is essential for the success of clinical trials. A thorough solution for handling trial information facilitates seamless data entry and the creation of Case Report Forms (CRFs). It accommodates complex, multi-center studies while significantly speeding up data validation and processing. The system also boasts multilingual support, allowing for global deployment in both cloud-based and on-premise environments. Clinical researchers are acutely aware of the need to minimize costs and time during trials, particularly regarding the collection and management of specific study data. In the past, study coordinators relied on paper CRFs to ensure that critical patient information was recorded and conveyed to sponsors for analysis. However, those times are now a thing of the past. The industry has shifted towards electronic data capture (EDC) systems, which enhance efficiency and elevate the quality of the collected data. By adopting these modern systems, researchers can focus more on their core activities while ensuring accurate data management.

Flask Data empowers teams involved in life science research and development by providing them with timely clinical data and effective solutions aimed at ensuring patient safety. The Flaskdata.io cloud API platform simplifies the data collection processes for a variety of stakeholders, including patients, researchers, site coordinators, connected devices, and pharmaceutical companies. Our services in data management and safety oversight are crafted to reduce risks associated with the integrity of clinical data, the safety of patients, and adherence to established protocols. The Flaskdata.io platform is designed to be both automated and scalable, ensuring it can adapt to the unique needs of your clinical trials. As a technology company specializing in clinical data oversight and management, Flask Data stands out for its commitment to providing optimal solutions that guarantee high-quality clinical data while placing a strong emphasis on patient safety. Understanding that each clinical trial presents its own set of challenges, we focus on comprehensively grasping the specific issues you face. By fostering a collaborative relationship with your team, we aim to develop customized solutions that not only fulfill your requirements for high-quality clinical data but also enhance patient safety, thereby contributing significantly to the success of your research projects. Ultimately, our dedication to innovation and collaboration ensures that we remain a valuable partner in your clinical endeavors.

SymmetricDS is an innovative solution tailored for the replication and synchronization of data across databases and filesystems. It facilitates smooth data integration through ongoing change data capture, which allows for updates to occur nearly in real time, letting users focus on their applications without interruptions. This software has proven its reliability and speed in environments that require efficient database replication across both local and expansive networks. Moreover, its data capture capabilities excel in cloud settings and in scenarios where network bandwidth is limited or connectivity is unstable. By utilizing this robust tool, organizations can maintain the consistency and availability of their data, overcoming various challenges they might encounter. Ultimately, SymmetricDS empowers users to optimize their data management practices while ensuring operational continuity.

Dacima Clinical Suite stands out as a cutting-edge web-based platform that integrates electronic data capture (EDC), clinical data management software (CDMS), and clinical trial management tools into a single cohesive solution. Tailored for a variety of applications, it effectively supports clinical trials, epidemiological research, web randomization, electronic patient-reported outcomes (ePRO), surveys, and patient registries. The suite features three essential modules: the Manager (Administrator), the Designer Module, and the Data Entry Module, each playing a vital role in streamlining the research process. This comprehensive approach ensures that users have all necessary tools at their fingertips for efficient data management and analysis.

Data MATRIX provides an all-encompassing SaaS platform tailored specifically for clinical trial management. Established in 2009, the Data MATRIX team has focused on the intricate processing and analysis of clinical data, producing documentation that adheres to the regulations set forth by the Russian Ministry of Health, FDA, and EMA. Our innovative software simplifies the clinical trial workflow, enabling users to effectively oversee and monitor their progress through an online interface. Prior to the initiation of any project, we ensure to thoroughly adjust and validate our software, taking into account every detail necessary for peak performance. With a successful history of completing 180 projects for various pharmaceutical companies, biotech enterprises, and contract research organizations, our solutions have contributed to 6 of the top 10 Big Pharma firms achieving a notable 15% decrease in research and development costs. The commitment of our dedicated team extends beyond projects as they are actively engaged with professional networks that link clinical data professionals such as CDISC, ACDM, SCDM, biostatisticians like ISBC, and medical writers affiliated with EMWA and AMWA. By consistently refining and advancing our offerings, we strive to foster innovation within the clinical research sector, ensuring that our solutions remain at the forefront of industry needs. This commitment to progress not only supports our clients but also enhances the overall landscape of clinical trials globally.

DFnet is a healthcare technology firm that focuses on providing eClinical solutions, including electronic data capture, eSource, and extensive data management services. We enhance clinical trials on a global scale by offering greater flexibility, superior data quality, and increased efficiency. Our platform facilitates data collection from diverse sources, such as paper CRFs, EDC, and other electronic systems, as well as through online and offline tablet entries and ePRO. Users have the option to implement our system on-site or take advantage of our secure cloud hosting services. Our cutting-edge optical recognition technology accelerates both SDV and RBM processes, greatly minimizing the time necessary for manual data entry. Tailored for maximum versatility in multi-center studies, our web-based data capture system ensures that information from any source is easily accessible in a centralized real-time platform. This feature empowers researchers to make swift and informed decisions, ultimately enhancing the overall execution of clinical trials and leading to better outcomes. Additionally, our commitment to innovation means we are constantly evolving our solutions to meet the changing needs of the healthcare landscape.

Unlock the potential of electronic data capture with FormsCenter from Medforce Technologies, a software solution designed to enhance how businesses gather and manage information. FormsCenter simplifies the process of acquiring essential data, ensuring that all collected information is accurate and reliable. This platform allows for the centralized storage of large datasets, significantly reducing the risk of overlooking critical details. Furthermore, users can easily export their data in various formats, tailored to meet specific requirements. Recognizing that data is fundamental to your business's success, FormsCenter facilitates an efficient approach to capturing and utilizing vital information. Wave goodbye to handwritten forms and the burdensome task of repetitive data entry, as you no longer need to navigate through disorganized, manual spreadsheets. You are empowered to determine the precise information your business demands, utilizing an extensive toolbox that enables you to create and customize forms according to your unique needs. With FormsCenter, data collection and monitoring is achieved in a precise, consistent, and compliant manner, addressing the needs of both external stakeholders and internal team members, which ultimately boosts productivity and enhances data integrity. This groundbreaking system not only fosters improved decision-making capabilities but also cultivates a more methodical approach to data management throughout your organization, paving the way for future growth and success. By integrating FormsCenter, you can elevate your data strategies and streamline your operations like never before.

Sofpromed focuses on delivering electronic data capture (EDC) solutions specifically designed for firms in the biotechnology, pharmaceutical, and medical device industries that conduct clinical trials across all phases, from I to IV. The EDC system functions as a software platform that streamlines the processes of data collection, validation, and exportation during clinical research. Used worldwide, Sofpromed's EDC software supports a wide array of therapeutic areas, including oncology, hematology, cardiovascular health, metabolic disorders, central nervous system challenges, dermatology, infectious diseases, respiratory issues, and pain management, among others. Its intuitive and user-friendly design allows for swift data entry and straightforward navigation, enhancing user experience. The platform is equipped with essential features like access control and data encryption, ensuring the security of sensitive information. As a fully web-based system, it eliminates installation requirements, promoting both convenience and efficiency. Additional benefits include daily data backups and consistent service reliability, making it a dependable option for users. The system's compatibility across numerous devices, browsers, and operating systems further enhances its usability. It also encompasses integrated monitoring, data management, and reporting tools that maintain compliance with HIPAA, GCP, and 21 CFR regulations. Furthermore, Sofpromed provides a straightforward monthly flat-rate billing structure, which adds to its practicality for various clinical trial requirements. Overall, the combination of its extensive features and focus on user experience establishes it as an indispensable asset for the effective and compliant execution of clinical studies. By adopting such a versatile tool, organizations can improve the quality and efficiency of their data management processes.

Clinion EDC stands out as the leading Integrated Electronic Data Capture System in the field, enhancing the efficiency and quality of clinical trials. This advanced software accelerates the clinical trial process by minimizing deployment times, expediting data collection, ensuring timely study completion, and facilitating early data lock, all while maintaining cost-effectiveness and safeguarding high standards of data quality, integrity, and security. With Clinion EDC, all essential functionalities are seamlessly combined into a single platform, simplifying everything from study setup to data management and reporting. The integration of these features not only streamlines workflows but also significantly improves overall project outcomes.

OCR Gateway stands out as a top-notch OCR solution designed to enhance your document management processes. With OCR Gateway, you can effortlessly retrieve data from various sources, build robust workflows, and work seamlessly with your team. By utilizing this tool, you can prioritize essential tasks and eliminate the need for tedious manual data input. Embrace efficiency and streamline your operations to achieve better productivity.