Alternatives to GraphPad Prism

OpenClinica is a leading provider of clinical data management software solutions. OpenClinica provides powerful tools to ensure that clinical trials are compliant and efficient. OpenClinica Enterprise, OpenClinica Participate and OpenClinica Randomize are the core products.

In a matter of hours, you can create an eCRF that is just as easy to use and as simple as a paper one. This will help you avoid the most common problems in data collection for Pre-authorisation and post-authorisation studies. When creating an eCRF, make sure you have an EDC that is flexible. This will allow you to adapt to any type of study. The EDC includes a number of monitoring and management tools that will help you save a lot of time and effort in managing and monitoring the study. You should use a valid system that gives trust to the sponsor and allows for the collection of high quality data. Do not wait until the analysis phase to find errors in the data. Otherwise, you will have to chase down investigators to correct them. Avoid making the process of creating an eCRF long and complicated.

Origin is the preferred data analysis and graphing tool for more than half a million engineers and scientists in government and commercial laboratories around the world. Origin has an intuitive interface that is easy to use for beginners. You can also customize the program as you get more familiar. Origin graphs and analysis results can automatically adjust to data changes or parameter changes. This allows you to create templates or perform batch operations directly from the user interface without programming. Install free Apps from our website to extend the capabilities of Origin. Connect to other applications like MATLAB™, LabVIEW™, or Microsoft(c) Excel. Create custom routines in Origin with our scripting and C languages. OriginPro takes data analysis to the next level. OriginPro provides advanced analysis tools in addition to all the features of Origin.

Igor Pro 8 serves as an interactive platform for exploring scientific and engineering data, as well as for creating high-quality graphs and layouts suitable for publication. Since its launch in 1989, it has been embraced by tens of thousands of professionals in various technical fields. The software merges robust tools with a user-friendly point-and-click interface for casual users, while also offering a programming environment that caters to advanced users. Additionally, Igor Pro’s plugin capabilities enhance its core functionalities, allowing for custom tools tailored for data acquisition, instrument control, and complex computational tasks. The recent release of Igor Pro 8 introduces hundreds of enhancements, featuring 20 new operations, five new functions, and a new NetCDF XOP, making it even more versatile. For a comprehensive overview of all the updates, you can check the detailed list provided. This continuous evolution ensures that Igor Pro remains relevant and effective in addressing the needs of its diverse user base.

NuVerve is a collaborative SaaS that offers Scientific Data Intelligence for scientists. It provides a set easy-to-use features to structure data, create custom analyses, and automatically generate reports. NuVerve, priced at $75/month, is available to all scientists.

MedCalc is a statistical package for biomedical research. Statistics includes more than 220 statistical tests and procedures, as well as graphs and methods, including ROC curve analysis and method comparison, and quality control tools.

Welcome to Dotter.science, your go-to online resource for enhancing clinical research. Designed specifically for researchers and organizations conducting health research protocols, Dotter enables you to efficiently execute your study while concentrating on what truly matters. You can effortlessly collect and analyze your clinical research data, making the entire process smoother. With Dotter.science, you can quickly create customized data collection forms and enhance the efficiency of your clinical research databases, simplifying both statistical analysis and publication efforts. Targeted at researchers, healthcare professionals, and students, Dotter significantly improves time management and operational efficiency. Features of Dotter include optimized data collection through an intuitive graphical interface for designing your electronic logbooks (eCRF), allowing for rapid patient inclusion with real-time data consistency checks. Moreover, Dotter's streamlined statistical analysis means you can say goodbye to paper records! Your data is securely stored on certified servers throughout your study and can be easily exported in structured formats, ensuring that your research is both safe and accessible. This platform is not just a tool; it's a comprehensive solution for modern clinical research needs.

The AcqKnowledge Demo software serves as an efficient tool for simulating the recording of physiological data across numerous systems and transducers while offering a comprehensive range of functions. It features sample data files showcasing recordings from various sources, including MP Research Systems, BioHarness, Mobita, B-Alert, Epoch, and Stellar systems, representing both human and animal subjects. This Demo software emphasizes the key functionalities of the AcqKnowledge platform, utilizing the provided sample data files for demonstration purposes. Users can explore specific segments, gather measurements, and conduct analyses seamlessly. Additionally, the AcqKnowledge Demo boasts an intuitive Startup Wizard interface that allows easy access to sample data files and pre-configured graph templates, enhancing the user experience and facilitating efficient data exploration.

Protocol First not only connects disparate locations and dismantles barriers in Clinical Research during the pandemic, but its offerings remain valuable during regular times as well. What was once viewed as optional technology has now become essential. Our solutions facilitate ongoing communication, enabling research not just to persist but to thrive and progress at an accelerated pace. Featuring a fully integrated remote monitoring tool equipped with automatic tagging, our system operates seamlessly with any EDC, anytime, and from any location. Protocol First prioritizes the integration of Sites, Sponsors, CROs, and various functional areas to create a cohesive research environment. We provide holistic solutions that tackle the numerous challenges faced in Clinical Research. The foundation of Protocol First is ensuring accuracy and proper placement of your data, which increasingly incorporates AI, NLP, and ML technologies. A critical component of utilizing AI effectively is establishing a robust structure for your data. The suite of software offered by Protocol First guarantees that data flows efficiently from patients to the FDA, maximizing the potential of data science and enhancing the overall research process. As we move forward, our commitment to innovation will continue to evolve, further amplifying our impact in the field.

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

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

If you are engaged in clinical research, you are likely aware that gathering data can be a significant drain on your time and can easily become disorganized, particularly when relying on paper forms. This is precisely why we developed Teamscope: to streamline the process of collecting research data, ensuring its security while allowing for instant analysis. Our goal is to alleviate your concerns regarding research data management, giving you more freedom to focus on the aspects of your work that you truly enjoy. Transitioning from paper-based data collection to an electronic system with Teamscope is quick and straightforward. Our online form builder enables you to tailor your survey forms using 11 different types of fields. Additionally, the skip logic feature allows you to reveal or conceal fields based on user input, thus facilitating the creation of dynamic survey paths. With skip logic, you have the flexibility to design intricate pathways tailored to your research needs, and our team of specialists is available to assist you in constructing even the most sophisticated forms on Teamscope. Ultimately, this innovative tool not only enhances your data collection experience but also empowers your research endeavors.

EGI's Net Station 5.4 software suite serves as a versatile platform designed for a fully integrated and networked experience in EEG, electrical source imaging, and neuromodulation, enabling your laboratory to expand and evolve. This software boasts remarkable speed and performance, facilitating rapid data processing, while featuring a streamlined dashboard for effective data review and analysis, along with an intuitive interface that simplifies learning and user training. Additionally, it is designed to be expandable, allowing for the inclusion of source imaging and neuromodulation capabilities, and ensures compatibility with external hardware and software. A notable addition is the EEGLAB plug-in, which enhances interoperability with the GES High-Density EEG System, marking the first step in a series of open-source tools aimed at making high-density EEG accessible to a wider research audience. With Net Station 5.4 Acquisition, the process of capturing EEG data is now more efficient than ever; users can easily select montages, configure filters, verify impedances, and add events directly from the main interface, streamlining the entire workflow. This innovative approach not only improves productivity but also empowers researchers to more effectively analyze and interpret their data.

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

Castor serves as an Electronic Data Capture system tailored for medical research purposes. Designed by researchers specifically for their peers, Castor provides a user-friendly, comprehensive, and cost-effective solution that encompasses all essential functionalities typically expected from an EDC, along with additional innovative features. Among its standout capabilities are the ability to create eCFR forms independently, randomization processes, ePro for patient surveys, monitoring tools, seamless data import and export options, an EHR data importer based on HL7 FHIR, audit trails, and user management systems, among many others. This extensive suite of tools ensures that researchers can efficiently manage their data collection and analysis processes.

Medidata's Rave EDC (Electronic Data Capture) stands out as the premier system for managing clinical trial data from sites, patients, and laboratories with unparalleled sophistication and security. Serving as the foundation of the Medidata Clinical Cloud™, it offers a comprehensive platform that integrates various processes, thereby eliminating the need for data reconciliation and providing insightful data analysis across different studies and functions. Users can efficiently oversee their roles, studies, and sites from a centralized dashboard that spans all Rave EDC and other Medidata Clinical Cloud products. This system helps in avoiding the pitfalls of duplicate study master data and inconsistencies, such as varying IDs for the same sites across different applications. At the core of Medidata’s cohesive approach to Clinical Data Capture and Management, Rave EDC facilitates the seamless aggregation and reconciliation of data from diverse sources, including Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging, and Sensor Cloud; it also enhances data review and analysis through advanced tools like Rave TSDV and Medidata Detect. With these capabilities, Rave EDC not only simplifies data management but also empowers clinical researchers to make informed decisions based on reliable and comprehensive data insights.

Our platform offers a web-based interface designed for the efficient collection of data from various types of studies and clinical scenarios. Thanks to its adaptable and user-friendly data entry methods, data can be tailored to suit any medical specialty, patient demographic, or research initiative. The system enhances care quality by monitoring patient-reported outcomes and leveraging population analytics. Its secure, web-based design ensures compatibility with both personal computers and tablets, facilitating seamless data input. Researchers benefit from real-time reporting capabilities, enabling them to oversee the complete study process for both single and multi-site research, independent of their geographical settings. The DADOS Platform features an exceptional user interface (UI) and intuitive tools that empower clinicians and researchers to design programs or studies that effectively connect research and clinical practice. Patients find DADOS appealing due to its straightforward usability and accessibility from anywhere, making it a valuable tool in modern healthcare. Ultimately, this innovative platform fosters a collaborative environment where research and patient care can thrive together.

CORE (Clinical On-demand Research) provides a variety of specialized services that encompass the design, development, and management of electronic forms utilized in clinical trials both in the UK and internationally. In addition to crafting the necessary forms, CORE facilitates randomization, oversees data management, and supplies crucial study statistics, ensuring researchers have access to essential information. This organization is instrumental in collecting important data for those in both academic and commercial research environments. CORE has established a successful collaboration with FormsVision, which began under an FP7 EU funding initiative, and has implemented the ALEA eCRF (electronic Case Report Form) to enhance trials conducted in the UK and New Zealand. The dedicated team at CORE stands ready to provide an array of services, including database construction for CRFs, management of randomizations, drug supply coordination, and ePRO (ALEA). Furthermore, they offer data hosting solutions for various types of files, as well as expert guidance on funding applications, statistical support, and protocol writing advice. This comprehensive suite of services positions CORE as a vital partner in advancing clinical research efforts.

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

Minimize the daily manual tasks that occupy your time to concentrate on delivering outstanding services. Thread’s ABA data collection tool empowers your clinical teams to efficiently care for clients, manage programs, and swiftly handle data collection and ABA graphing, all within a single platform. By offering a user-friendly mobile solution, you can assist your direct care teams in addressing the challenges of on-the-go client care, making their responsibilities more manageable. Access client data sheets quickly for both online and offline data collection, enabling the tracking of intervals, percent correct, duration, task analysis, as well as real-time graphing and reporting to enhance the quality of clinical care provided to clients. Designed for ease of learning, Thread’s intuitive application allows ABA practices and clinical teams to start using it in as little as an hour, letting them prioritize what truly matters—achieving practice success while providing exceptional care. With such efficiency, your teams can also find more time to engage with clients on a personal level, further enhancing the overall quality of service.

As a provider specializing in Data Management, we deliver comprehensive services that include both data management and the planning and development of statistical analyses alongside suitable CRF design. We ensure that all necessary documentation complies with FDA standards and other relevant regulations. Our previous experiences indicate that investing more time in the planning stage significantly enhances the overall efficiency and speed of the trial's final phases. Our databases are meticulously created by seasoned data managers who possess extensive knowledge of various eCRFs and understand the essential aspects of electronic data capture system design and data collection. This expertise enables us to construct the eCRF in a remarkably short timeframe. Additionally, the validation and testing of the eCRF are critical components of our design process, handled by separate personnel to guarantee a thoroughly detailed and functional eCRF. By prioritizing these elements, we can ensure the highest quality outcomes for our clients.

KoboToolbox offers a range of tools designed for the collection of field data in demanding situations. Our platform is completely free and open-source. The majority of our users include individuals engaged in humanitarian efforts, as well as aid workers and researchers operating in underdeveloped regions. Our development and research teams are located in Cambridge, MA, along with various other locations worldwide. Rapidly gathering dependable information during a humanitarian crisis, particularly after a significant natural disaster like a major earthquake or typhoon, is essential for protecting the lives of those most at risk. Unfortunately, the urgent needs of the affected population are often overlooked due to the lack of efficient methods for collecting and analyzing vital data. To fill this critical gap, KoboToolbox was established as a free and open-source resource for data collection and analysis during humanitarian emergencies and other difficult contexts. Our initiative relies entirely on the generous support of grants and collaborations with our partners, ensuring that we can continue to provide these vital tools to those who need them most. By facilitating quick access to actionable insights, we aim to empower communities to respond effectively to crises.

Clinical research is a time-consuming and demanding task. This puts a lot of pressure on the project team and makes it difficult to manage everything. The solution was designed to save you time when it comes to electronic data capture in clinical trials. Our data management department provides everything you need to collect clinical data. This will allow you to spend your time on what is most important. We can implement non-usual features or unique project-specific requirements. The EDC system is also flexible in budget terms. It is well-suited for low-budget clinical research. Our team has fully configured the Electronic Data Capture tool to meet your project requirements. Don't waste your time on system validation and configuration. The EDC system source code as well as the database are stored in the European Datacenter, or in any other country you choose. Multilevel backup also ensures the safety of clinical data.

Management of clinical data. Comprehensive solution for managing clinical trial information. Easy data entry and creation of CRFs. Support for multi-center complex studies. Data validation and processing is accelerated Multilingual capabilities. Global deployment, cloud-based and on-premise. Clinical researchers understand the importance of reducing time and costs when conducting clinical trials. This is especially true when it comes to the collection, processing, and management of study-specific data. To ensure that the necessary patient data was recorded and sent to the sponsor for analysis and processing, study coordinators used paper Case Report Forms (CRFs). The days of paper CRFs are long gone. The industry now understands that electronic data capture (EDC), systems increase efficiency and improve data quality.

Manage your clinical trials data effortlessly and with sophistication. Clincase’s e-Clinical Technology Solutions present a comprehensive suite of features, services, and additional functionalities accessible through a single login. This robust and flexible EDC software ensures that data managers, monitors, and sponsors stay interconnected with the study's performance and advancements, while also promoting greater participation from sites and investigators. Clincase delivers user-friendly, efficient solutions that provide real-time data accessibility. As a zero-footprint solution, it utilizes secure and encrypted data transfers for protection. The clinical trial data is securely hosted in Germany, conforming to the highest physical security standards. Our architecture is fully redundant, guaranteeing that data is continuously mirrored to a secondary data center for added reliability, with full backups conducted daily, ensuring data integrity and availability. With Clincase, you can streamline your clinical trials process and enhance collaboration among all stakeholders involved.

Data management is crucial to the success and efficiency of your clinical research. Despite being complex, Quanta View, an e-CRF, makes it possible to control the processing of your data. Quanta View includes elements such as monitoring, follow up of inclusions, and project management. The application will be there to help you in all aspects of your clinical research. It is accessible via the internet and responsive. It adapts to all media (tablet, laptop, etc.). Quanta view is designed for the pharmaceutical, medical device, and cosmetic industries.

ActiView is a comprehensive acquisition software that enables users to visualize all ActiveTwo channels simultaneously while storing the data in .BDF format on a network disk. Its interface is intuitively designed to allow for a rapid assessment of data quality. This tool is versatile, facilitating the acquisition of EEG, ECG, and EMG signals, in addition to integrating data from extra sensors such as the AnalogInputBox (AIB), digital triggers from the USB2 receiver, and various additional sensors connected to the AD-box, including those for respiration, GSR, temperature, ergometers, and plethysmography. A range of filtering options, reference selections, and downsampling capabilities are available to enhance the user experience. With our unique single buffered method, the software ensures stable and reliable data acquisition even during multitasking, utilizing DMA transfer to a large intermediate ring-buffer to prevent data loss effectively. ActiView is an open-source program developed in LabVIEW, providing researchers with a flexible tool that they can modify and enhance based on their specific needs and creative ideas. This adaptability makes it especially valuable for scientists looking to tailor software functionality for their research projects.

Cloudbyz EDC, a cloud-native application with an intuitive user interface, is designed to store and effectively manage clinical data throughout the life cycle of a clinical trial. Our innovative solution allows clinical research teams the ability to collect, analyze and manage clinical data that is of varying complexity and size. Create your study without coding, using an interface that allows users to create forms and navigate easily to the appropriate screens for data analysis and collection.

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

LifeSphere EDC offers a budget-friendly solution for sponsors and CROs to efficiently gather, manage, and report clinical trial data, regardless of the trial's stage or complexity. By consolidating various systems into one cohesive database, it eliminates the necessity for expensive integrations and data reconciliation processes. The platform captures clinical information directly from study sites, thereby removing the reliance on paper Case Report Forms (CRFs) and manual data entry. This approach not only shortens study development timelines but also facilitates smooth implementation of adjustments in ongoing studies. Integrated with the LifeSphere Clinical cloud platform, which includes LifeSphere eTMF and LifeSphere EDC, it effectively links operations with data oversight. Additionally, the single sign-on feature simplifies access to a comprehensive suite of applications, while its open architecture promotes swift integration with external applications through APIs. This level of efficiency ensures that clinical research can adapt quickly to changing demands and maintain high-quality data standards.

When compared to other Electronic Data Capture (EDC) solutions available from companies like MediData, DataTrack, and Omnicomm, TrialStat stands out as the most comprehensive suite of study management tools that can effortlessly integrate with various external data sources, including electronic medical records (EMR), wearable devices, and both clinical and non-clinical information systems. TrialStat presents a cohesive platform that caters to all phases and categories of clinical trials. Our EDC suite is designed with a single sign-on feature and supports multiple tenants, incorporating modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, a Vendor Neutral Imaging Archive, an extensive Reporting and Analytics Portal, and tailored Machine Learning applications. With an emphasis on data analysis, TrialStat provides real-time reporting capabilities, on-demand data extracts, and analytics that span a single study, a program, or the entirety of your research portfolio, ensuring that all stakeholders receive pertinent, customized, and timely insights into every facet of study data while pinpointing areas of risk or potential delays. Additionally, the platform’s integration capabilities allow for improved collaboration among research teams, fostering a more efficient and effective trial management experience.

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

Any organization that accepts checks as a payment method stands to gain from utilizing AQ2 Remittance. This versatile solution is designed to accommodate businesses that handle a minimum of 25 to 50 checks daily, scaling up to manage hundreds or even thousands of transactions. By leveraging advanced check capture technology, businesses can experience substantial reductions in operational and labor expenses. AQ2 Remittance facilitates the swift electronic transmission of check images along with pertinent information, eliminating the need for couriers or frequent trips to local bank branches. Additionally, the burdensome costs associated with manually recording check amounts on deposit slips, conducting manual research, and distributing hard copies become obsolete. This comprehensive check capture and electronic deposit solution is tailored for businesses, allowing for seamless data capture that can be uploaded directly into your accounts receivable system. The efficiency and convenience of AQ2 Remittance can transform how companies manage their check payments.

Med-Quest's innovative method of data collection offers substantial time savings for you and your team. By enabling the extraction of data straight from medical devices, the time you save can be quantified in days and hours rather than merely in minutes and seconds. With Med-Quest, you won't be hindered by unnecessary features or inundated with excessive information. The aim of Med-Quest is to ensure a user experience that remains straightforward and focused. By eliminating unused tools, you can dedicate your attention to your essential tasks. Med-Quest is ideally suited for projects of any scale, whether local or international, providing comprehensive support. With the ability to access your data from virtually anywhere, you can utilize it effectively no matter your location. Securely obtain your data online at any research facility or from the comfort of your home. Ease the burden on both your team and participants by allowing them to input data directly from a tablet on their couch or a smartphone while on the move, ultimately transforming the data collection process into a more efficient experience. This flexibility not only enhances productivity but also improves engagement from participants.

Easily create mobile surveys that provide automated reporting in real-time; BizEfficiency equips decision-makers with comprehensive analyses and insights about their operations. Capture essential events with features like photo uploads, signatures, GPS tracking, and all necessary form fields. We foster a continuous partnership with your business to promote consistent growth. Our platform offers online capabilities, auto-save features, and ensures data integrity, meaning your information is never compromised. This guarantees accurate process management and valuable reporting to support proactive decision-making. With our service, you can quickly design mobile forms and start gathering information from any mobile device within minutes. Building mobile data collection forms is straightforward, and these can be utilized on both smartphones and tablets. Employees can gather a wide variety of data, including images, barcodes, and more, available for collection anytime, whether they are online or offline. Once forms are submitted, real-time analysis becomes immediately accessible, allowing you to make informed decisions without delay. This innovative approach streamlines your operational efficiency and enhances your overall data management strategies.

Formic's versatile technology facilitates the rapid and scalable collection of multichannel patient experience surveys, serving over 200 NHS and public sector clients to transform patient feedback into actionable insights, assist with GP revalidation, and lay the groundwork for both immediate and long-term enhancements in quality and service. Our patient experience software can be deployed onsite, hosted, or offered as a fully managed solution, ensuring data validation at the point of entry while providing swift, accurate, and reliable results across both paper and digital mediums. Supporting a variety of formats including paper, online, tablets, kiosks, and touchscreens, Formic is designed to synchronize surveys across different channels, ensuring that responses from multiple organizations are consistent and aggregated into a central database, simplifying the process of analysis for care providers in various health and care environments. This comprehensive approach not only enhances the accuracy of data capture but also significantly streamlines reporting procedures for healthcare professionals.

Unlock unique insights with unparalleled freedom and adaptability using LabChart physiological data analysis software, which seamlessly integrates all your recording devices, enabling the simultaneous acquisition of biological signals from diverse sources while applying sophisticated calculations and visualizations in real time during your experiments. Quickly determine metrics such as Mean Arterial Pressure, Systolic Pressure, and Max dP/dt from your blood pressure recordings in mere moments. The Blood Pressure module offers remarkable ease of use and delivers rapid results, while our intuitive two-point calibration tool simplifies the conversion of voltage units to recognized measurement units efficiently. LabChart is designed to handle essential tasks effortlessly, with advanced functionalities remaining unobtrusive until they are needed. Tailor LabChart to your preferences by utilizing scripting and automation features available on Windows, and leverage custom arithmetic along with import and export capabilities across various formats for compatibility with other software applications. Experience a new level of efficiency and precision in your physiological data analysis with LabChart.

Kickstart your project by selecting one of our applications as a base for customization and configuration. If you don't find the right fit, you can always build a new application from the ground up using our user-friendly visual designer. Equipped with robust pre-built components, you have the flexibility to create forms, establish workflows, and design your application through an easy drag-and-drop interface, all without the need for coding! Utilize the intuitive visual designer to develop your study, structuring your database to align with the specific type of research and data collection required. You can easily aggregate and examine your data through tailored screens, ensuring that you can identify discrepancies, manage incomplete submissions, and track follow-ups efficiently. Reorganize your database into easily manageable segments based on your selected criteria, and create filters using natural language for enhanced accessibility. Additionally, leverage saved datasets for comprehensive reporting, workflow management, patient tracking, and in-depth data analysis, ultimately streamlining your project’s processes and improving efficiency.

ExpiWell’s exceptional data collection platform, endorsed by numerous researchers globally, effectively tackles the limitations of conventional survey techniques. By utilizing Ecological Momentary Assessment (EMA) and Experience Sampling Method (ESM), it captures real-time data from the world while ensuring outstanding participant engagement. This platform allows for a comprehensive observation of participants' experiences through instantaneous data gathering. It enhances interaction between researchers and participants, leading to greater involvement in the research process. With ExpiWell’s ESM capabilities, research transforms from a mere static process into a dynamic interaction, enabling seamless participant rewards, community building, and immediate feedback. By merging the strengths of ESM with community-centric research approaches, ExpiWell empowers you to nurture connections, promote social support, and enhance engagement within your participant network. This innovative approach enables researchers to deliver timely solutions that can drive meaningful change in their organizations or communities effectively. Ultimately, ExpiWell is revolutionizing the way data is collected and utilized in research, paving the way for more impactful outcomes.

Mosio allows research teams to improve subject adhesion, communications, data collection, and communication on mobile's most popular channel, text messaging. Our software helps research teams communicate more efficiently with participants by delivering interactive elements to mobile phones and messaging automation. WHO CAN WE HELP? + Clinical Trial Sponsors (Pharma & Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers/Directors and Clinical Operations Managers/Directors. Clinical Project Managers. Principal Investigators. Clinical Research (Study). Coordinators. All research staff who regularly communicate with study participants. BENEFITS + Interactive medication reminders and medication compliance alerts + Automate data collection. + Increase engagement and adherence. + Get SMS appointment reminders to fix your no-show problem. + Increase retention with automated check ins

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

Achieve a comprehensive understanding of your research operations by utilizing a robust and standardized clinical trial management system that has been developed in partnership with prominent academic medical and cancer centers. Streamline billing designation processes to promote uniformity across various teams and systems. Enhance your budgeting strategies, ensure accurate routing of charges, and perform more effective audits and monitoring of billing compliance. This integrated approach provides deep visibility and insight into all elements of clinical research, particularly in financial management, thanks to collaboration with elite research institutions. Moreover, by connecting OnCore with your existing electronic medical records (EMR), including seamless integrations with Epic and Cerner, you can significantly boost patient safety, minimize redundant data entry, improve billing compliance, and elevate overall operational efficiency. Ultimately, this system not only simplifies processes but also fosters a more effective research environment.

SlimEDC serves as a cloud-based solution for Electronic Data Collection (EDC), enabling the seamless initiation of both retrospective and prospective studies, including patient studies (ePRO) and market research projects, through its user-friendly study editor. Users can choose between a fully managed software option overseen by the research sponsor or a more comprehensive service where a dedicated team from SlimEDC manages the entire process, culminating in data evaluation. Specifically designed to comply with EU regulations and standards, SlimEDC ensures that respondents are engaged electronically while the software automatically generates all necessary reports mandated by regulatory bodies. Additionally, SlimEDC maintains compliance with ISO 9001 and 27001 standards, highlighting its commitment to quality and security. Our team is certified by BHBIA and has completed specialized training in pharmacovigilance to enhance our expertise. Furthermore, strict GDPR audits conducted by independent entities guarantee that our legal and data security measures meet the highest standards, ensuring the protection of sensitive information throughout the research process. By prioritizing both compliance and user experience, SlimEDC positions itself as a reliable partner in the realm of electronic data collection.

Dacima Clinical Suite, the most advanced web-based solution, combines electronic data capture (EDC), medical data management software (CDMS) and clinical trial management software into one platform. Dacima Clinical Suite is designed for clinical trials, epidemiological studies, web randomization, ePRO, surveys, and patient registers. Dacima Clinical Suite comprises three core modules: the Manager (Administrator), Designer Module, and the Data Entry Module.

Open HealthHub represents the pioneering platform for fully encrypted communication between healthcare providers and patients. We prioritize the security and privacy of your information above all else, consistently adhering to the General Data Protection Regulation (GDPR). This commitment is what we refer to as "secure by design." The Open HealthHub offers a streamlined method for healthcare professionals and researchers to gather patient information safely and efficiently through a mobile application or medical devices. Our integration capabilities, which utilize APIs and adhere to global medical data standards like FHIR and SNOMED CT, ensure seamless incorporation of the Hub into the existing systems of any hospital or medical facility. This innovative approach not only enhances data collection but also fosters trust between patients and their healthcare providers.

GoResearch™ is an advanced and thoroughly validated online platform designed for electronic data capture (EDC), developed by 2KMM specifically for research initiatives like clinical and observational studies as well as patient registries. It boasts a comprehensive suite of features that facilitate these projects across multiple domains, including the customization of data flow and management of Adverse Events procedures, which includes automatic email alerts to safety teams. Additionally, it allows for random assignment to treatment groups via its integrated randomization module, enables data collection through tailored electronic case report forms (eCRF) to align with the specific needs of each study, and supports the integration of ePRO, eSource, and mHealth data through specialized mobile or web applications, as well as a versatile application programming interface (API). This platform ultimately aims to enhance the efficiency and accuracy of data management in research contexts.

DSG, Inc., a global leader in eClinical, offers a complete suite of innovative technology solutions as well as data management services to the global clinical research community. DSG's eClinical platform offers a competitive advantage and on-time delivery. DSG solutions have been used in thousands clinical trials across the globe using our award-winning eCaseLink™, platform and eCaseLinkDesign for enterprise licensing. The company was founded in 1992 and is proud to have been awarded the SCDM Data Driven Innovation Award.

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

DiData is a web-based software solution that can be customized to meet the needs of clients. It currently has three main uses: -Laboratory stock management (Di-Freeze) -Electronic Data Capture System, (Di-EDC). -Laboratory Information Management System, (Di-Lims). Some of its key features: Blazing fast rendering and proven usability on large data sets - Rapid deployment: Integrate with your existing systems/instruments quickly thanks to the available libraries and REST API Data view features: Use filters, edit columns, and highlighter to get the best view of your data. Dashboard : This module can be customized to meet your specific needs. Our website lists more main features and benefits in-detail.

Viedoc designs engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We believe in life and science, in people, and in our collective power to change the world and build a healthier future. That unmatched driving force is what pushes us to innovate, accelerate and improve every aspect of modern clinical studies. Since 2003, Viedoc has united scientists and clinical trial professionals in a shared mission of pushing life-changing research forward. Our solution has been used to power thousands of studies, by collecting data from over a million patients and allowing it to flow smoothly across sites and countries. We take great pride in helping bridge the gap between patient and researcher – and, in the best of cases, between research and breakthrough.