Top UNITY Alternatives

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.

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.

Since 2005, Medrio's Electronic Data Capture (EDC) platform and its complementary eClinical solutions like ePRO, RTSM, eConsent, and Direct Data Capture (DDC) have gained the trust of leading pharmaceutical, biotech, CRO, animal health, medical device, and diagnostic organizations. Our reputation is built on providing user-friendly solutions that enhance the efficiency and simplicity of clinical trials across all phases, sizes, and complexities. Users of Medrio can create their databases in an average of 2.8 weeks without needing any programming skills and can easily implement mid-study modifications with just a few clicks. With options ranging from add-on features to comprehensive service packages, Medrio delivers adaptable, modular solutions tailored to meet the precise needs of our clients, ensuring they receive only the services they require. Our cutting-edge software, combined with extensive training and support resources, has resulted in a remarkable 98% customer satisfaction rating, demonstrating our commitment to excellence in the clinical trial landscape. We continuously strive to innovate and improve our offerings to keep pace with the evolving needs of our users.

Within just a few hours, you can design an electronic Case Report Form (eCRF) that is as user-friendly and straightforward as its paper counterpart. This approach will significantly reduce the typical challenges encountered in data collection for both pre-authorisation and post-authorisation studies. When you set out to create an eCRF, it’s crucial to utilize an Electronic Data Capture (EDC) system that offers flexibility, enabling you to customize it for various study types. Additionally, the EDC comes equipped with several monitoring and management tools that can greatly streamline the study oversight process, saving you both time and energy. It is essential to employ a reliable system that instills confidence in the sponsor and facilitates the gathering of high-quality data. Addressing any data errors only during the analysis phase can lead to complications, as it may require you to track down investigators for corrections after the fact. Therefore, strive to keep the eCRF creation process efficient and straightforward, ensuring that it meets all necessary requirements without unnecessary complexity. By focusing on these elements, you can enhance the overall effectiveness and accuracy of your 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.

ClinCapture aims to develop software that has the potential to save lives. Their innovative technology not only lowers the expenses associated with clinical trials but also enhances the efficiency of data collection while ensuring the confidentiality of patient information. Additionally, ClinCapture serves as a comprehensive platform that supports the assessment and advancement of drugs, biologics, and medical devices, which can address a diverse range of health issues. By prioritizing both cost-effectiveness and patient privacy, ClinCapture is dedicated to improving the overall landscape of clinical research.

Mosio empowers research teams to enhance participant engagement, streamline communication, and gather data effectively through the widely used medium of text messaging. Our platform offers research teams the tools to interact more effectively with participants via mobile devices, integrating engaging elements and automated messaging features. WHO CAN BENEFIT? + Sponsors of clinical trials in the pharmaceutical and biotech sectors + Cancer treatment facilities and organizations focused on clinical research + Studies funded by the National Institutes of Health (NIH) + Agencies dedicated to public health + Professionals such as clinical trial managers, directors, project managers, principal investigators, and coordinators, along with all research personnel involved in participant communication. ADVANTAGES + Engaging medication reminders and alerts for compliance + Automation of the data collection process + Boost in participant engagement and adherence rates + SMS reminders for appointments to reduce no-show rates + Improved participant retention through automated check-ins, ensuring ongoing communication and support. Overall, Mosio serves as a vital tool for enhancing the efficiency of clinical research endeavors.

As a specialist in Data Management, we provide a wide array of services that encompass not only data management but also the strategic planning and development of statistical analyses along with appropriate CRF design. We take care to ensure that all required documentation adheres to FDA regulations and other pertinent guidelines. Our past experiences have shown that dedicating additional time to the planning phase can significantly improve the efficiency and speed of the trial's concluding stages. Our databases are crafted with precision by experienced data managers who have a deep understanding of various eCRFs and the crucial elements involved in designing electronic data capture systems and collecting data. This level of expertise allows us to develop the eCRF in an impressively short period. Furthermore, the validation and testing of the eCRF are vital components of our design process, performed by specialized personnel to ensure a comprehensive and functional eCRF. By emphasizing these critical aspects, we guarantee exceptional quality outcomes for our clients, fostering a collaborative relationship built on trust and results. Ultimately, our commitment to excellence positions us as a leader in the field of data management services.

Mahalo Health is a comprehensive digital health platform designed to accelerate the development of patient-centered digital health solutions and clinical trials. It offers an array of prebuilt modules that enable the rapid deployment of customizable white-label applications tailored to specific therapeutic areas. The platform is equipped with advanced data capabilities, which include a predictive health engine for anticipating diseases and diagnoses, a behavior modification engine that promotes healthy patient habits, and a notification system that guarantees prompt communication via push notifications, SMS, or emails. Mahalo Health is dedicated to upholding rigorous security and compliance standards, adhering to regulations like HIPAA, GCP, ISO27001, and GDPR. Its diverse service offerings span various therapeutic domains, such as diabetes management, cognitive health, cardiovascular care, musculoskeletal issues, mental well-being, oncology, rare diseases, and nonalcoholic steatohepatitis (NASH). Furthermore, Mahalo Health not only enhances patient engagement but also improves health outcomes by equipping healthcare providers with innovative digital tools and solutions that adapt to the evolving needs of their patients. This commitment to innovation ensures that healthcare delivery is both efficient and personalized.

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.

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.

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.

Gain a thorough grasp of your research functions by implementing a comprehensive and standardized clinical trial management system that has been crafted in collaboration with leading academic medical and cancer institutions. Optimize billing designation workflows to facilitate consistency across different teams and platforms. Refine your budgeting methodologies, guarantee precise charge routing, and conduct more efficient audits and monitoring of billing compliance. This cohesive strategy offers extensive visibility and understanding of all facets of clinical research, especially in financial oversight, due to partnerships with top-tier research organizations. Additionally, by linking OnCore with your current electronic medical records (EMR), including smooth integrations with systems like Epic and Cerner, you can greatly enhance patient safety, reduce redundant data entry, improve billing compliance, and increase overall operational effectiveness. This advanced system not only streamlines processes but also cultivates a more productive research atmosphere, ultimately leading to improved outcomes in your clinical initiatives. Furthermore, the integration of these advanced technologies may lead to a more collaborative environment among research teams, fostering innovation and excellence.

Replior stands out as an innovative company that focuses on delivering advanced software solutions tailored for clinical trials, featuring a comprehensive platform that integrates EDC, eConsent, ePRO, and Virtual Visits to optimize trial execution. Our all-encompassing system, known as Trial Online, streamlines the collection and management of data from researchers, participants, and wearable technology efficiently. It is meticulously designed to support decentralized clinical trials (DCT), providing the flexibility to accommodate site visits, remote interactions, or a blend of both. Our journey began two decades ago when we were tasked with developing an online CRF service for a prominent pharmaceutical company, which marked our evolution from an IT operations provider into a specialized software developer focused on clinical data collection. Over time, we have broadened our offerings to provide a full range of data collection services, while our IT operations are adeptly overseen by our highly skilled sister company, Complior. As we forge ahead, our unwavering commitment to innovating and improving clinical trial processes remains central to our purpose, driving us to continually enhance user experience and data integrity in the trials we support.

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.

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.

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.

TrialKit is a versatile cloud-based solution accessible through a web interface and a dedicated mobile application, designed to facilitate comprehensive clinical trial management for organizations involved in medical devices, diagnostics, digital therapeutics, and biopharmaceuticals, regardless of their scale. With our user-friendly study builder, you can create and launch validated studies in just days instead of weeks, eliminating the need for any programming knowledge. To date, numerous users worldwide have utilized the adaptability of TrialKit to successfully launch more than 8,000 studies spanning all stages of development. This platform empowers researchers to streamline their processes and enhance the efficiency of clinical research endeavors.

A reliable and intuitive cloud-based Electronic Data Capture (EDC) platform designed to oversee clinical trials and studies, regardless of their scale or complexity, encompassing features like electronic patient-reported outcomes (ePRO), electronic consent (eConsent), electronic clinical outcome assessments (eCOA), electronic source data (eSource), patient-reported outcome measures (PROMs), patient-reported experience measures (PREMs), functional health assessments, and tools for participant education and engagement. This versatile platform enhances the efficiency of research processes, ensuring that both researchers and participants have a seamless experience throughout the study.

EvidentIQ's eCOA simplifies the process of gathering real-time data directly from patients via an intuitive interface, which not only improves patient evaluations but also elevates the quality of data collected. Clients can opt for a comprehensive eCOA package or customize their selection by combining different components to meet specific requirements. By arranging a demonstration with our expert team, you can learn how to optimize the return on investment for your research initiatives. The eCOA platform integrates data science services with advanced technology, offering a flexible solution. It functions independently of specific eClinical technologies such as EDC systems, while also providing smooth integration with current eClinical software environments. This system is designed to efficiently collect a diverse array of outcome data from patients, healthcare professionals, or observers, ensuring compliance and improving the data collection experience overall. With its adaptable nature, organizations can tailor the eCOA framework for various clinical trial situations, thereby significantly enhancing their research capabilities and outcomes. Such customization not only meets immediate needs but also prepares teams for future challenges in clinical research.

Mednet is an innovative eClinical technology firm dedicated to delivering healthcare solutions tailored for the worldwide life science community. Their adaptable, EDC-focused eClinical platform enhances the efficiency of clinical research, regardless of project size. Mednet offers a complete suite of solutions equipped with all essential tools for the creation and management of clinical studies, while also being flexible enough to meet evolving demands and standards. For nearly two decades, Mednet has earned the trust of Contract Research Organizations across all sectors of the pharmaceutical, medical device, and biotechnology fields. They deliver the expertise, dependability, and creativity crucial for success in research endeavors. For further details, visit Mednetsolutions.com, where you can explore a wealth of information about their offerings and capabilities.

Enhance the efficiency of your clinical studies with Clinvigilant, your global provider of budget-friendly eClinical tools tailored for CROs, Pharma, Biotech, Nutraceuticals, and academic institutions throughout both clinical and post-marketing phases. Our clients consistently choose to partner with us due to our: ♦ Rapid EDC implementation (under 4 weeks). ♦ Cost-effective solutions. ♦ Integration capabilities with third-party and legacy systems. Our cloud-based platform, hosted on Microsoft Azure, adheres to HIPAA, ICH-GCP, GDPR, and 21 CFR part 11 regulations and has successfully undergone audits by the FDA, EMA, and MHRA. The Clinvigilant eClinical suite encompasses a variety of tools, including EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent, and eCOA. You can select the specific tools you require, and we will seamlessly integrate them into your existing software framework. Each interaction and data exchange generates detailed Audit Trails, ensuring real-time visibility of compliant data across all relevant roles. Our offerings are modular, highly customizable, and accessible via web, iPad, and mobile applications for both Android and iOS platforms. Additionally, we support the use of Patient's Own Devices (BYOD) and can interface with various devices and wearables for enhanced data collection. With Clinvigilant, you can count on a comprehensive solutions provider to streamline your clinical trial processes effectively and efficiently. Your success in clinical research begins here.

Signant Health stands as a global frontrunner in evidence generation, dedicated to revolutionizing the clinical trial landscape by engaging patients in their own settings and reimagining the path to validation. They provide a comprehensive suite of clinical technology solutions that encompasses electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician evaluations, and an integrated eClinical platform. Their offerings also include patient engagement tools like an intuitive app, eConsent for effective informed consent practices, and telehealth capabilities. Furthermore, Signant Health specializes in clinical data and analytics services, which involve COA data analysis along with the synthesis and interpretation of data. With over thirty years of experience, the company has been crucial in facilitating numerous clinical trials and has significantly contributed to hundreds of drug approvals, solidifying their position as a dependable partner for sponsors and CROs who aim to deliver high-quality data for informed decision-making and regulatory filing. Their unwavering dedication to innovation is continuously molding the future of clinical research, ensuring that advancements benefit both patients and the medical community at large.

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.

Flex Databases offers a cutting-edge, integrated, and compliant electronic clinical platform that delivers software solutions tailored for clinical trials, serving pharmaceutical companies and contract research organizations (CROs). Our comprehensive system includes a Clinical Trial Management System, an Electronic Trial Master File, a project management and budgeting tool specifically crafted for the clinical trials sector, a Pharmacovigilance System, and a Learning Management System. This adaptable platform was developed through the expertise of a skilled team of over 100 professionals who possess extensive knowledge of the complexities involved in the clinical trial process. Additionally, our commitment to innovation ensures that we continually evolve our offerings to meet the changing needs of the industry.

DSG, Inc., a prominent name in the eClinical space, provides an extensive range of cutting-edge technology solutions alongside comprehensive data management services tailored for the international clinical research sector. With its eClinical platform, DSG delivers both a competitive edge and ensures timely project completion. Their innovative solutions have facilitated numerous clinical trials worldwide, leveraging the acclaimed eCaseLink™ platform and eCaseLinkDesign for enterprise-level applications. Established in 1992, the company proudly holds the SCDM Data Driven Innovation Award, highlighting its commitment to excellence in the industry. DSG continues to evolve and enhance its offerings, demonstrating its dedication to advancing clinical research methodologies.

Jumpstart your project by choosing one of our applications as a foundation for your customization and configuration needs. Should you not discover a suitable option, you have the opportunity to create a new application entirely from scratch with the help of our intuitive visual designer. This designer comes equipped with a range of powerful pre-built components, giving you the freedom to construct forms, set up workflows, and craft your application via a simple drag-and-drop interface, all without writing any code! Make use of the user-friendly visual designer to design your study, tailoring your database to meet your specific research and data collection requirements. You can effortlessly gather and analyze your data through customizable screens, which allows you to spot inconsistencies, handle incomplete submissions, and monitor follow-ups with ease. Organize your database into easily manageable segments based on your chosen criteria, and create filters using natural language for improved accessibility. Furthermore, take advantage of saved datasets for thorough reporting, workflow management, patient tracking, and extensive data analysis, ultimately optimizing your project’s procedures and enhancing overall productivity. With these tools at your disposal, you can ensure that your project runs smoothly and effectively.

If you're involved in clinical research, you probably recognize that collecting data can be a considerable time sink and may lead to disorganization, especially when using paper forms. This challenge is what inspired the creation of Teamscope: a solution designed to simplify the data collection process while ensuring its security and enabling immediate analysis. Our objective is to ease your worries about managing research data, allowing you to concentrate on the areas of your work that you find most fulfilling. Moving from traditional paper-based methods to an electronic system like Teamscope is both fast and easy. With our online form builder, you can customize your survey forms using a variety of 11 field types. Furthermore, the skip logic feature allows you to manage which fields are displayed based on users' answers, making it simpler to create dynamic survey paths. Through the use of skip logic, you can craft complex pathways that cater specifically to your research requirements, and our team of experts is ready to help you develop even the most elaborate forms on Teamscope. In conclusion, this cutting-edge tool not only improves your experience in collecting data but also enhances the effectiveness of your research efforts, ultimately contributing to better outcomes in your studies. By adopting Teamscope, you are taking a significant step towards modernizing your data collection practices.

Jeeva has developed a revolutionary modular system that operates on a cutting-edge cloud platform. With just one login from any device that supports a browser, users can easily screen patients, offer education, manage enrollment, send SMS and emails, and compile evidence such as electronic patient-reported outcomes. Frustrations with slow patient recruitment and retention are common in the industry, making it imperative to gather solid evidence of safety and efficacy for new investigational medicines to secure approval from regulatory agencies. Jeeva stands out as an invaluable resource for optimizing time and financial resources for patients and biopharma sponsors, particularly in long-term follow-up studies associated with gene therapy. Its innovative approach streamlines processes, ultimately enhancing the efficiency of clinical trials and improving patient care.

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.

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.

Cloudbyz EDC is a cloud-based application featuring a user-friendly interface that facilitates the storage and management of clinical data throughout the entire clinical trial process. This cutting-edge solution empowers clinical research teams to gather, analyze, and oversee clinical data of diverse complexities and sizes. Users can design their studies without the need for coding, utilizing an interface that makes it simple to create forms and access the necessary screens for data gathering and analysis. Overall, Cloudbyz EDC streamlines clinical research workflows, enhancing efficiency and accuracy in data management.

The merging of eCOA with digital technology is revolutionizing the landscape of clinical research, creating a bridge between conventional practices and cutting-edge, patient-focused methodologies. Opt for YPrime's eCOA solutions to secure not only superior patient data but also to improve the overall experience for sponsors, investigator sites, and patients. Utilizing a versatile software development approach, YPrime can rapidly customize and modify features to align with specific study needs within a remarkable 8 to 12-week timeframe. Our dynamic and visually appealing design process enables clients to assess the system at different phases of development, keeping them well-informed prior to the system's launch. Moreover, our pre-validated and adaptable authoring environment not only expedites startup timelines but also allows for modifications after production, such as protocol changes, thereby becoming an essential resource for clinical research. This dedication to flexibility and responsiveness solidifies YPrime's status as a frontrunner in the changing world of clinical trials, ensuring that we remain at the forefront of innovation in the field. In doing so, we strive to enhance the efficiency and effectiveness of clinical studies, ultimately benefiting all stakeholders involved.

Axiom has developed Fusion, a unique and affordable eClinical platform designed specifically for small to medium-sized companies in the device, pharmaceutical, and biotech sectors. This comprehensive eClinical Suite offers customizable Modules tailored to your study’s specific requirements. If you are conducting a smaller study, you can select a foundational setup that includes Electronic Data Capture (EDC) and Data Management (DM), along with Adverse Event (AE) and Serious Adverse Event (SAE) tracking. For those seeking enhanced functionalities, Fusion provides advanced Modules such as Inventory Tracking, Randomization and Trial Supply Management (RTSM), and Safety Management to streamline study oversight. The platform also facilitates the electronic collection of study data, even in offline scenarios, ensuring that once an internet connection is available, your information seamlessly syncs with the Fusion databases. This capability enables real-time access to records relevant to subject screening activities, while the Fusion Safety Database effectively supports the management of pharmacovigilance events for improved patient safety. Overall, Fusion stands out as a versatile solution to meet diverse clinical trial needs.

Omda MedSciNet solutions significantly improve the quality, usability, and management of medical data throughout its entire lifecycle, encompassing everything from data collection to analysis. This secure and standardized platform simplifies the process for clinical researchers and professionals in both healthcare and academic settings, facilitating the efficient gathering and analysis of well-structured medical data. The dedicated team at Omda is proficient in creating and managing tailored database applications, in addition to designing clinical studies specifically aimed at advancing medical research and quality registries. The Omda MedSciNet study platform provides a reliable, feature-rich, and highly flexible online environment that is ideal for hosting and managing intricate study and clinical trial systems. With a successful history of over two decades, Omda MedSciNet has adeptly supported studies and clinical trials of diverse scopes and sizes. Standard implementations include a wide range of essential components required for launching fully operational studies or trials, ensuring that researchers are equipped with all the necessary tools. This unwavering commitment to quality and customization not only enhances the user experience but also solidifies Omda MedSciNet's position as a frontrunner in medical data management, continuously evolving to meet the needs of the research community. By prioritizing innovation, Omda MedSciNet remains at the forefront of advancements in the healthcare data landscape.

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.

Introducing Dotter.science, the ultimate online platform dedicated to advancing clinical research. Specifically crafted for researchers and organizations involved in health research protocols, Dotter allows you to focus on the essential aspects of your study while executing it efficiently. The platform facilitates the seamless collection and analysis of clinical research data, making the entire experience more streamlined. With Dotter.science, you can swiftly design personalized data collection forms, enhancing the effectiveness of your clinical research databases and simplifying both your statistical analysis and publication processes. Aimed at researchers, healthcare practitioners, and students alike, Dotter is designed to significantly boost time management and operational productivity. Among its features are optimized data collection capabilities through a user-friendly graphical interface for creating electronic logbooks (eCRF), which enables quick patient enrollment complemented by real-time data consistency checks. Additionally, with Dotter’s efficient statistical analysis, you can leave traditional paper records behind! Your data will be securely stored on certified servers throughout the duration of your study, and you can conveniently export it in structured formats, guaranteeing that your research remains safe and easily accessible. This innovative platform stands as more than just a tool; it is a comprehensive solution tailored to meet the multifaceted demands of contemporary clinical research, ensuring you are well-equipped for success in your endeavors.

The Datimbi Platform is expertly crafted for situations that necessitate the collection of large amounts of detailed and organized data from multiple sources or contributors, incorporating built-in quality assurance features and the capability to monitor and manage quality and collection activities in real time, along with thorough reporting and analytical tools. Additionally, a swift setup process is one of the standout features of our platform. It is specifically designed for uses such as electronic Case Report Forms (eCRFs) in Clinical Trial Management, Social Case Management, econometric event study assessments, or nearly any data collection and processing workflow that prioritizes efficiency. If your needs correspond with these scenarios, you can frequently achieve complete deployment and operational readiness on the platform in as little as one week! Establishing roles, updating workflow statuses, crafting intricate data collection forms, setting processing rules, managing value lists, monitoring changes, and generating custom email alerts can all be performed through an easy-to-use web interface. Moreover, these capabilities can be managed by your own trained staff or through services provided by Datimbi, offering both flexibility and support tailored to your organization's requirements. This blend of quick deployment and user-friendly design makes the Datimbi Platform an indispensable tool for any project that relies heavily on data. With its robust features, teams can streamline their data management processes and enhance overall productivity significantly.

CORE (Clinical On-demand Research) offers an extensive range of specialized services that include the design, development, and management of electronic forms used in clinical trials across the UK and globally. Beyond creating the essential forms, CORE also manages randomization processes, data oversight, and provides vital study statistics, ensuring that researchers have the key information they need. This organization plays a critical role in gathering significant data for both academic and commercial research sectors. Notably, CORE has formed a successful partnership with FormsVision, which originated from an FP7 EU funding initiative, and has integrated the ALEA eCRF (electronic Case Report Form) to improve trial execution in the UK and New Zealand. The dedicated team at CORE is prepared to deliver a wide range of services, which encompass database development for CRFs, management of randomizations, coordination of drug supplies, and ePRO (ALEA) solutions. They also provide data hosting services for various file types and offer expert assistance with funding applications, statistical analysis, and protocol development. By delivering this comprehensive array of services, CORE solidifies its role as an essential collaborator in the progression of clinical research initiatives. Their commitment to enhancing research methodology and data integrity further underscores the importance of their contributions to the field.

Open HealthHub stands as a groundbreaking platform facilitating fully encrypted communication between healthcare practitioners and patients. Our utmost priority is safeguarding your personal information, and we strictly comply with the General Data Protection Regulation (GDPR), embodying our principle of being "secure by design." The Open HealthHub provides an efficient means for healthcare professionals and researchers to securely collect patient data via a mobile application or medical devices. Furthermore, our robust integration capabilities leverage APIs and conform to internationally recognized medical data standards such as FHIR and SNOMED CT, allowing for effortless integration of the Hub into the current systems of any healthcare facility. This cutting-edge approach not only improves the process of data collection but significantly enhances the trust that patients place in their healthcare providers, fostering a more collaborative environment for health management. Ultimately, Open HealthHub is dedicated to revolutionizing the way healthcare communication is conducted, ensuring that both security and efficiency are at the forefront of patient-provider interactions.

Our platform for managing clinical trials is engineered to support virtually any form of controlled clinical trial, including randomized studies, and provides a range of randomization algorithms. This versatile software can be easily configured for both paper Clinical Report Forms (CRFs) and electronic CRFs (eCRFs). It is adept at capturing data in various formats and methods, adhering to the specific guidelines you set to maintain data integrity and quality assurance. The system allows for direct Electronic Data Capture (EDC) via eCRFs, or it can generate paper CRFs that can subsequently be entered into the system. Additionally, users can upload a variety of media including images, audio recordings, videos, and documents such as consent forms, with the only constraint being the available storage space. The platform incorporates Double Data Entry and offers thorough exception reporting to ensure accuracy. Furthermore, it features a mechanism to lock records once they have been validated, preventing any further modifications. This extensive functionality significantly bolsters the reliability of the data gathered throughout the trial, thus enhancing the overall research quality. Overall, our platform is designed to streamline the clinical trial process while ensuring the highest standards of data management and security.

Clinicubes CTMS is a powerful and efficient clinical trial management system tailored for hospitals, site management organizations, and smaller contract research entities, with a strong focus on finance tracking, budget management, and detailed reporting. This platform is equipped with a host of useful features that streamline the management and execution of every aspect of clinical trials. By centralizing the trial database, it guarantees access to the most up-to-date information, significantly boosting overall productivity. The system facilitates the aggregation, organization, and reconfiguration of data pertaining to physicians and healthcare service providers. Furthermore, it allows for the systematic collection, assessment, and analysis of data gathered from multiple studies across different sites, bringing together findings into an integrated report. It includes robust reporting functionalities that evaluate trial execution against predefined criteria and goals, providing a clear overview of progress. Additionally, users benefit from interactive dashboards that present study performance metrics and operational insights, enabling teams to stay informed and proactive. In conclusion, this sophisticated CTMS not only enhances decision-making processes but also ultimately leads to improved trial outcomes and efficiency.

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.

We are your partner in advancing clinical trial technology, working collaboratively to elevate the entire trial experience. Our innovative software solutions are designed not only for efficiency but also prioritize meaningful personal connections. By partnering with you, we aim to ensure that your upcoming trial surpasses all expectations. The study setup is streamlined, taking just a few days to complete; you can choose to let us handle it or take charge of the setup yourself. Data collection is flexible, allowing either investigators or subjects to lead, and it is compatible with any device for ease of use. Our application is thoughtfully designed to incorporate all essential features in a seamless and intuitive format. We are committed to helping you meet both your regulatory requirements and business objectives. A dedicated professional will be available to address any questions you might have, providing timely and effective solutions. Currently, we are focused on supporting medical device companies in achieving their compliance and business goals with precision. Together, let’s revolutionize your clinical trial experience and set new standards for success.

AnjuEPS emerges as a leading solution for eSource and site automation, dedicated to improving the efficiency of early-phase clinical trials from the volunteer recruitment stage all the way to study submission. By directly capturing data from medical devices and utilizing real-time edit checks, it guarantees a high standard of data accuracy while minimizing the dependency on paper documentation. The system prioritizes volunteer safety by providing immediate alerts for any values that fall outside the normal range and leverages historical safety data to enable proactive safety management. Its intuitive Design & Build Module streamlines the study creation process, effectively reducing both time and costs. Key features include customizable reporting options, sample tracking tailored to complex pharmacokinetic and pharmacodynamic processes, as well as comprehensive modules for both recruitment and pharmacy management. Additionally, AnjuEPS is dedicated to upholding the integrity of clinical data collection through principles of accuracy, transparency, and efficiency, thereby fostering the overall success of clinical trials. In a landscape where the demand for reliable and efficient clinical trial processes is ever-increasing, AnjuEPS positions itself as an invaluable asset for research teams.

Phoenix CTMS is a cutting-edge web application that combines the capabilities of database software crucial for clinical research into a unified modular framework. Following thorough collaboration with trial sites at the Medical University of Graz, this innovative platform is now publicly accessible under the LGPL 2.1 license. Its remarkable suite of features caters to the operational and regulatory requirements of the clinical front end in academic research, as well as for CROs and hospitals conducting clinical studies across various phases. For those in search of a CDMS that supports extensive JavaScript form scripting on both server and client sides, this system stands out as an excellent choice. It adeptly manages large electronic case report forms (eCRFs), serving as a strong open-source alternative for users who require eCRF functionality. Moreover, its capability to generate complex ad-hoc database queries aids in the identification of appropriate subject candidates through set operations, while also simplifying the management of multiple trials at once, thereby ensuring the effective organization of site personnel and resources. Additionally, the software supports the implementation of diverse processes that comply with ICH GCP guidelines, solidifying its role as a comprehensive solution for clinical trial management and enhancing its utility in a rapidly evolving research landscape.

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.

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.

CSAM Studies, previously referred to as MedSciNet Studies, is a powerful and flexible online platform that has effectively facilitated the management of clinical research for the past twenty years. This internet-based resource for medical studies offers an extensive array of applications aimed at the hosting, administration, and supervision of projects of various sizes and complexities. CSAM MedSciNet's standard offerings encompass all critical components needed to launch a fully functional study or clinical trial. Moreover, this exemplary solution is enhanced with features that support dynamic and interactive data entry forms, customizable workflow designs, and advanced tools for data validation, analysis, and exportation. By utilizing these capabilities, researchers can adopt a thorough and efficient strategy for overseeing their clinical trials. As a result, CSAM Studies continues to evolve, meeting the changing demands of medical research with innovative solutions.

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.