Alternatives to CORE (Clinical On-demand Research)
Compare CORE (Clinical On-demand Research) alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to CORE (Clinical On-demand Research) in 2024. Compare features, ratings, user reviews, pricing, and more from CORE (Clinical On-demand Research) competitors and alternatives in order to make an informed decision for your business.
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OpenClinica
OpenClinica
OpenClinica is a premier provider of clinical data management software solutions. Offering powerful tools for efficient, compliant clinical trials, OpenClinica helps maximize the security, reliability, and compliance of every clinical research. Core products include OpenClinica Enterprise, OpenClinica Participate (helps capture data directly from study participants), and OpenClinica Randomize. -
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Medrio
Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM). Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services. Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating. -
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ClinCapture
ClinCapture
At ClinCapture our mission is to build software that saves lives. Our technology lowers the cost of clinical trials by streamlining data capture processes while providing a platform that protects patient privacy. Clincapture advances the evaluation and development of drugs, biologics, and devices that demonstrate promise for the diagnosis and/or treatment of a wide range of diseases or medical conditions. -
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GoResearch
2KMM
GoResearch™ is a fully validated, innovative internet platform for electronic data capture(EDC) created by 2KMM for research projects such as clinical/observational studies andpatients registries. It offers a wide range of features supporting such projects invarious areas such as: configuration of the information flow and the Adverse Events management procedures (including automatic e-mail notifications to safety departments), random allocation to a treatment arm through the built-in randomization module, data collection with the use of individually customized case report forms (eCRF) to meet the requirements of each study, and ePRO, eSource and mHealth data integration through dedicated mobile and/or web applications or flexible application programming interface (API). -
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Dacima Clinical Suite
Dacima Software Inc.
Dacima Clinical Suite is the most advanced web-based solution that combines electronic data capture (EDC), clinical data management software (CDMS), and clinical trial management software in a single platform. Built for clinical trials, epidemiological research, web randomization (IWRS), ePRO, web surveys, and patient registries, Dacima Clinical Suite helps efficiently streamline the clinical data collection process. Dacima Clinical Suite consists of three core modules: Manager (Administrator) Module, Designer Module, and Data Entry Module. -
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Prelude EDC
Prelude
Prelude is the investigator's preferred EDC system. Built with the end-user in mind, Prelude is the most user-friendly data capture system in clinical research. Focus on what really matters, and spend less time training sites and users in entering, QA'ing, and extracting data from the database. When you work with Prelude, our Customer Success Managers become an extension of your team to help make the database build and support as easy as possible. Additional product offerings include ePRO, Offline, and eConsent. 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. -
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Dotter.science
KerNel Biomedical
Welcome to Dotter.science, the online platform to support clinical research. Intended for researchers and organizations piloting health research protocols, Dotter allows you to be supported in carrying out your study and to stay focused on the essentials. Collect and analyze your clinical research data with ease. On Dotter.science, easily create collection forms and optimize the entry of your clinical research databases, in order to facilitate statistical analysis and publication. Aimed at researchers, professionals and health students, Dotter saves time and efficiency. Dotter features. Optimized data collection. Design your electronic logbooks (eCRF) on our user-friendly graphical interface, and quickly start including your patients with our real-time data consistency checking tools. Simplified statistical analysis. With Dotter, you no longer need paper! Your data is secured on certified servers for the duration of the study, and easily exportable in structured formats -
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Castor EDC
Castor
Castor is an Electronic Data Capture system for medical research. Built by researchers, for researchers, Castor is an easy to use, complete, and affordable solution that offers all the capabilities researchers expect from an EDC, and more. Top features include self service eCFR creation (form building), randomization, ePro (patient surveys), monitoring, easy import and export of data, EHR data importer (HL7 FHIR based), audit trails, user management, and much more.Starting Price: $100.00/year -
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Viedoc
Viedoc Technologies
Viedoc designs engaging software for the life science industry. By accelerating clinical trials on all levels, the Viedoc solutions support major pharmaceutical, biotech, and medical device companies, as well as renowned research institutions worldwide. Headquartered in Uppsala, Sweden, Viedoc also has offices in America, France, Japan, Vietnam, and China. Since Viedoc's inception in 2003, over 1 million patients in more than 75 countries have participated in studies powered by Viedoc. Specialities: Electronic Data Capture, ePRO, Randomization, Medical coding, Logistics, eCOA, reporting, and data managementStarting Price: Free Trial -
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DFdiscover
DFnet
DFnet is a healthcare technology company that provides eClinical solutions, including electronic data capture, eSource, and data management services. We bring more flexibility, better data quality, and greater efficiency to clinical trials everywhere in the world. Collect data from any source – paper crfs, EDC and other electronic sources, online/offline tablet and ePRO entries. Install within your controlled premises or allow us to host in our secure cloud environment. Accelerate SDV and RBM processes with advanced optical recognition that shaves time off manual data entry. Built for maximum flexibility of multi-center studies. Web-based data capture from any source is instantly available in a centralized real-time platform. -
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TrialMaster
Anju Software
The most intuitive Electronic Data Capture (EDC) Suite on the market featuring superior usability and flexibility, TrialMaster is your EDC solution for Phase I-IV clinical trials. TrialMaster improves efficiencies and reduces workflow impact while enhancing your data quality, resulting in faster study submission times. TrialMaster, with its built-in ePro , allows site researchers, patients self-reporting their outcomes and sponsor staff to access the platform from any device (desktop, laptop, tablet or smart phone). All system screens adapt in real-time to the size of the device. Single sign-on capabilities (SSO) allow sponsors to use their own IdP for authentication, reducing the need to maintain multiple user names and passwords. -
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Ennov EDC
Ennov
Clinical data management. A comprehensive solution to capture and manage clinical trial information. CRF creation and intuitive data entry. Support for complex, multi-center studies. Accelerates data validation and processing. Multilingual capabilities. Fit for global deployment, cloud-based or on premise. Every clinical researcher understands the importance of saving time and resources during the conduct of clinical trials. This is especially true when you consider the collection, processing and management of protocol-specific data for each study subject. In the past, study coordinators relied on paper Case Report Forms (CRFs) to ensure the required patient data was recorded and transferred to the sponsor for processing and analysis. Thankfully the days of paper CRFs are largely behind us as the industry understands that the use of electronic data capture (EDC) systems increases the efficiency of data collection and improves overall data quality. -
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OnCore
Advarra
Gain visibility into all aspects of your research operations with a comprehensive, proven, and standardized clinical trial management system built through collaboration with leading academic medical centers and cancer centers. Centralize billing designation information to ensure consistency across multiple teams and systems. Improve your budgeting process, route charges correctly, and conduct more accurate auditing/monitoring of billing compliance. Gain visibility and insight into all aspects of clinical research, including comprehensive financial management, with a standardized system built in collaboration with top research institutions. Integrate OnCore with your current EMR, including turnkey interfaces with Epic and Cerner, to increase patient safety, reduce duplicate data entry, enhance billing compliance, and increase operational efficiency. -
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TrialStat
TrialStat Solutions
Compared to other EDC solutions on the market from MediData, DataTrack, Omnicomm and others, TrialStat is the most all-encompassing suite of study management tools that can be seamlessly connected to external data sources such as EMR, wearables, and other clinical and non-clinical data and information sources. TrialStat offers a fully unified platform suitable for all phases and types of trials. Our single-sign-on, multi-tenant EDC suite includes modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, Vendor Neutral Imaging Archive, a robust Reporting and Analytics Portal and custom Machine Learning programs. With a focus on data analytics, TrialStat offers real-time reporting, data extracts on demand, and analytics across a single study, a program, or your entire research portfolio – providing all stakeholders relevant, customized, timely insight into all aspects of study data and highlighting areas of risk or potential delays. -
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Teamscope
Teamscope
If you are a researcher doing clinical research you know that data collection can be a huge time-drainer and mess, especially when using paper forms. That's why we created Teamscope: to help you easily collect research data, keep it secure and instantly analyse it. We want to help you worry less over your research data and have more time for the things you love. With Teamscope you can switch from collecting data on paper to electronically in no time. Use our online form builder to customise your survey forms with 11 different field types. Skip logic is a feature that makes it possible to hide or show fields depending on what values are entered. With skip logic you can create alternative paths or branches within a survey. The conditions that create each path can be as complex as you want to make them and our experts are ready to help you build even the most complex form on Teamscope.Starting Price: $87 per month -
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QureClinical
Quretec
As a Data Management provider we offer data management and statistical analysis planning and model development with applicable CRF design. All the appropriate documentation is provided by us according to FDA and other regulations. Previous experience has shown us that putting more effort into the planning phase will give a better, faster and efficient result in the end-phase of the trial. Our databases are generated by experienced data managers who have worked with several eCRF-s and already know the critical parts of the electronic data capture system design and data collection. This allows the eCRF to be built in a short period of time. eCRF validation and testing is compulsory part of the design and is dealt by different personnel in order to receive a hundred-percent elaborated eCRF. -
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UNITY
RAYLYTIC
AI-powered medical image analysis meets advanced clinical data process automation. Available as web-based SaaS or an on-premise solution, UNITY is trusted worldwide by major medical technology manufacturers and hospitals to collect complete, consistent, and compliant data. The integrated modules for PROM, eCRF, and medical image analysis streamline key data collection activities to enable faster, cost-efficient trials. RAYLYTIC's Imaging Core Lab possesses decades of experience in the high-precision, automated, independent evaluation of musculoskeletal morphology and device performance in spine, hip, and knee to offer clients unparalleled analytic and operational support. -
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ClinVigilant
ClinVigilant
Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. How simple and user-friendly is it? Ask for a demo to find out! Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials. Enquiries > bd (at) clinvigilant.com -
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Quanta View
Quanta Médical
We know that data management is essential to the success of your clinical studies. Although these remain very complex, it is currently possible for you to ensure the processing of your data thanks to Quanta View, the e-CRF which is perfected according to your expectations. Quanta view has elements such as the creation of eCRF, monitoring, follow-up of inclusions, project management. The application will accompany you from A to Z in your clinical research. Accessible on the internet and responsive, it adapts to all types of media (tablet, computer, etc.) Quanta view is intended for pharmaceutical industries, medical device industries, cosmetic industries, etc. Offer you a comprehensive clinical research service hub, flexible and adapted to a high-performance, demanding and constantly evolving ecosystem. -
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eCaseLink
DSG
DSG, Inc. is a leading global eClinical provider with a fully unified suite of innovative technology solutions and data management services for the global clinical research community. DSG's eClinical software platform provides competitive advantage that is cost-effective with on-time project delivery. DSG solutions have been used in thousands of clinical trials around the globe with our award-winning eCaseLink™ platform and eCaseLink Designer for enterprise licensing. Founded in 1992, the company is proud to be recognized as the first provider of a fully integrated EDC and IRT Randomization and Trial Supply Management system with the SCDM Data Driven Innovation Award. -
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Mosio
Mosio, Inc.
Mosio enables research teams to improve subject adherence, communications, and data collection on mobile’s most popular channel: text messaging. Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones. WHO WE HELP: + Clinical Trial Sponsors (Pharma and Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants. BENEFITS: + Interactive dosing reminders and medication adherence alerts. + Automate data collection. + Increase engagement and adherence. + Fix your no-show problem with SMS appointment reminders. + Improve retention with automated check-ins.Starting Price: $99/month -
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EDC Made Easy
XClinical
The software platform Marvin provides solutions for Clinical Data Management, such as EDC (including IWRS/Drug Management, WebPRO, reporting, etc.), Coding, Composer (CDISC ODM-based study design including SDTM mapping), SDTM visualization, Clinical Document Management (eTMF) and a mobile application for direct communication between Investigators & Patients. Our software and technical services accelerate clinical trials worldwide. XClinical is an international eClinical vendor founded in 2002. Its software platform Marvin provides solutions for Clinical Data Management, such as EDC (including IWRS/Drug Management, WebPRO, reporting, etc.), Coding, Composer (CDISC ODM-based study design including SDTM mapping), SDTM visualization, Clinical Document Management (eTMF) and a mobile application for direct communication between Investigators & Patients. Our software and technical services accelerate clinical trials worldwide. -
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Flask Data
Flask Data
Flask Data provides life science R&D teams with same-day clinical data and patient safety solutions. The Flaskdata.io cloud API platform unifies data collection apps for patients, researchers, site coordinators, connected devices, and drugs. Our data management and safety monitoring solutions help you reduce risk to clinical data, patient safety, and protocol compliance. The Flaskdata.io platform is automated, scalable, and adaptive to the needs of your clinical trial. Flask Data is a technology company specializing in clinical data management and monitoring. We are accomplished at providing our customers with the most effective way to achieve high-quality clinical data and assure patient safety. There is no single solution that works for every clinical trial. We work hard to understand your unique situation. We work with your team to develop the best solution to achieve high-quality clinical data and assure patient safety. -
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Cloudbyz EDC
Cloudbyz
Cloudbyz EDC is a cloud-native solution with an intuitive interface that is designed to store and manage clinical data effectively throughout a clinical trial’s life cycle. Our innovative solution enables clinical research teams to efficiently collect, analyze, and manage clinical data of different complexity and size. Build your study without code, with an interface that helps users build forms and easily navigate to the appropriate screens for data collection and analysis. ̌The all-new Cloudbyz EDC application comes packed with user-friendly features. All other Cloudbyz applications such as CTMS, eTMF, CTBM, RTSM and Safety/ PV are native to the same platform as our EDC, allowing customers to have one single source of truth for a clinical trial. Furthermore, you can set up each study independently. -
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OnlineCRF
OnlineCRF
We know that clinical research requires a lot of attention and time. This places a heavy load on the project team, and there is a big challenge to manage everything. We tailored the solution to save your time in tasks related to Electronic Data Capture in clinical trials. Our data management department creates everything you need to properly collect clinical data. This will help free up your time for what is important. We can implement non-usual features or unique project-specific requirements. It is even flexible from a budget perspective: the EDC system is perfectly fitted to low-budget clinical research. The Electronic Data Capture tool is fully configured by our team and perfectly complies with your project needs. Do not spend your valuable time on system configuration and validation. The EDC system source code and the database are stored in the European datacenter or in any other country that you choose. The safety of clinical data is also guaranteed by the multilevel backup. -
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Calyx
Calyx
At Calyx, we know that the success of your clinical development program comes down to data. Which makes the effectiveness of your electronic data collection (EDC) system key. Used in over 2,600 worldwide clinical trials, Calyx EDC streamlines clinical trial data collection and reporting—in one easy-to-use platform. Don’t trust your important data to just anyone. Contact us to learn how Calyx can propel your program’s success. Calyx EDC gives you the flexibility to easily plan, design, and conduct studies, regardless of their complexity. With features that help reduce costs, improve site visibility, and drive efficiency, Calyx EDC keeps your trial on track. -
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TrialKit
Crucial Data Solutions
Founded in 2010, Crucial Data Solutions (CDS) provides the most innovative low-code/no-code data and clinical trial management technology on the market today. TrialKit, our cloud-based platform available via both a web and native mobile app, enables end-to-end clinical trial management for medical device, diagnostics, digital therapeutics, and biopharm 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, including Verily (a subsidiary of Alphabet), ICON, Catalyst Clinical Research, SISCAPA Assay Technologies, CDx Diagnostics, and Optinose, and many more.Starting Price: Upon request -
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Sofpromed
Sofpromed
Sofpromed provides electronic data capture (EDC) systems for biotechnology, pharmaceutical, and medical device companies conducting phase I-IV clinical trials. An EDC system is a software tool used to collect, clean, and export data in clinical trials. Sofpromed’s EDC application is used in clinical trials worldwide across multiple therapeutic areas, including oncology, hematology, cardiovascular, metabolic, central nervous system (CNS), dermatology, infectious diseases, respiratory diseases, and pain, among others. Clear design, intuitive, and very easy to use. Quick data entry and navigation. Access control and data encryption. Fully web-based, no installations required. Daily data backups, seamless service. Works in multiple devices, browsers, and operating systems. Built-in monitoring, data management, and reporting tool. Meets HIPAA, GCP, and 21 CFR. Convenient billing model. monthly flat rate. -
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Clinion EDC
Clinion
AI-enabled and Integrated Electronic Data Capture (EDC) Software Clinion EDC is the most Integrated Electronic Data Capture System in the Industry making your clinical trials faster and better. Our Electronic Data Capture(EDC) Software accelerates the speed of your clinical trial by reducing deployment time, capturing data faster, timely study close-out, and early data lock – all in a cost-effective manner providing the highest data quality, integrity, and security. Clinion EDC Software integrates all the functionalities you need into one platform, from study setup to data management and reporting. What can you expect? - Quick mid-study changes, no need to rely on tech support or take your study offline. - Accelerates data validation and processing by using form rules like edit checks and skip logic. - Support for complex, multi-center studies - Can be integrated with Clinion RTSM, Clinion eCOA, and Clinion CTMS - easy-to-use interface and AI-enabled features -
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Rave EDC
Dassault Systèmes
Medidata’s Rave EDC (Electronic Data Capture) is the most advanced, robust and secure EDC system for clinical trial site, patient, and lab data capture and management. Rave EDC is the cornerstone of the Medidata Clinical Cloud™, the unified clinical research platform that connects processes, eliminates data reconciliation and delivers cross-functional and cross-study data insights. Centrally manage your users, roles, studies, and sites across all Rave EDC (and other products on the Medidata Clinical Cloud) studies. Eliminate study master data duplication and inconsistencies (e.g., different IDs for the same sites in different applications). Rave EDC is at the heart of Medidata’s unified solution for Clinical Data Capture and Management, enabling aggregation and reconciliation of data from multiple sources, Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging and Sensor Cloud; and intelligent data review and analysis with Rave TSDV and Medidata Detect. -
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LifeSphere EDC
ArisGlobal
Cost-effective data capture. LifeSphere EDC delivers sponsors and CROs a cost-effective way to capture, manage and report clinical research data regardless of trial phase and complexity. Combine disparate systems into a single unified database eliminating the need for costly integrations and reconciliation. Captures clinical data direct from site, eliminating the need for paper CRF and data entry. Reduce study development times and create seamless implementation of changes to live studies. Unified with the LifeSphere Clinical cloud platform – including LifeSphere eTMF and LifeSphere EDC – to seamlessly connect operations with data management. Single sign-on functionality provides simple access to a suite of applications, while open architecture ensures rapid integration with third party applications via API. -
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Entrypoint i4
Phoenix Software International
Entrypoint is a complete system for creating, deploying, and administering custom data entry applications, providing data entry and system administration access anywhere you are. Entrypoint is a suite of easy-to-use tools which allow users to design, deploy, and use a wide variety of custom data entry applications with built-in validation, editing, and export options. Entrypoint has many built-in attributes that make adding advanced features such as range checks and table lookups a simple operation. Collecting information on paper forms to re-enter it later into a computer system is a double-entry process that adds the risk of transcription errors and takes extra time. Entering data directly into a database via electronic forms eliminates the paper step. Switching to electronic data capture becomes an even more compelling choice for organizations who face an increase in data volume and rising costs. -
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Replior
Replior
An integrated EDC, eConsent, ePRO and Virtual Visit platform for the efficient conduct of clinical trials. Replior is a company providing software for clinical trials. Our suite of systems is called Trial Online and enables collection and management of data from investigators, participants and wearables in an easy and efficient way. Trial Online supports decentralized clinical trials (DCT) by enabling the trials to operate with site visits, remote visits or as a hybrid. We started our journey 20 years ago with a request to build an online CRF service for one of the world’s largest pharma companies, back then we were an IT operations provider for the pharma industry. This was the starting point of providing software for collection of data in clinical trials. Today we offer a full suite of data collection software services, and our IT operation is performed by our, very certified, sister company Complior. -
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SlimEDC
Altamira
SlimEDC is a cloud platform for EDC – Electronic Data Collection. Retrospective and prospective studies, patient studies (ePRO), and market research projects are ready to launch in no time, using the provided study editor. SlimEDC is available as software, that is fully managed by the research sponsor or as a complex service, where the entire process up to the evaluation of data is provided by a professional SlimEDC team. SlimEDC is adapted to the EU environment and legislation. The respondents are contracted electronically, the software generates all the legally required reports for regulatory organizations. SlimEDC is ISO 9001 and 27001 compliant. Our team is BHBIA certificated and has undergone pharmacovigilance training. The legal and data security is subject to strict GDPR audits conducted by independent authorities. -
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LibreClinica
LibreClinica
The real open source electronic data capture (EDC) for clinical studies. The project started with volunteers from different background, i. e. academia, clinical research service, IT industry and is currently in use at academic institutes, hospitals and companies/startups.Starting Price: Free -
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IBM® Clinical Development provides pharmaceutical, contract research organizations and medical device companies unified technology from start up to submission to support clinical trials. With our clinical data management system, users can organize and analyze report data from anywhere in the world. Enabling pharmaceutical organizations to deliver therapies faster to their patients. Design and launch studies without database migration. Deliver quick and easy remote consent with minimal integration.
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Mednet
Mednet
Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s flexible, electronic data capture (EDC)-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond simply EDC, Mednet’s comprehensive solution set provides the tools required to build and manage all types of clinical research, while adapting to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success. For more information, visit mednetsolutions.com. -
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Jeeva eClinical Cloud
Jeeva Informatics Solutions
Jeeva's patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience. Delays in patient recruitment & retention are keeping them up at night. Generating enough evidence of safety and efficacy of investigational new medicines is critical to get timely approval from regulatory agencies. Whether you are a patient group setting up a registry or natural history study, or a biopharma sponsor of a clinical trial, or a long-term follow-up study for gene therapy, Jeeva can save you time, and money while improving user experience for study team and trial participants.Starting Price: $100/mo/user -
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Data MATRIX
Data MATRIX
All-in-one diamond SaaS solution for clinical trials. Data MATRIX team has been working with clinical data since 2009. We process data, analyze it and develop documents to be accepted by the Russian Ministry of Health, FDA, and EMA. Our products automate the processes of clinical trials, and users manage and monitor its progress online. We adjust and validate our software before the project starts and take into account all aspects of the project in order to do it in the best way. Our team has conducted 180 projects for pharmaceutical and biotech companies and CROs. With Data MATRIX products, 6 out of 10 TOP Big Pharma companies reduced their R&D costs by 15%. Our employees are proud to be members of professional communities which unite clinical data specialists (CDISC), data managers (ACDM, SCDM), biostatisticians (ISBC), and medical writers (EMWA, AMWA). -
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clincase
Quadratek Data Solutions
Conduct your clinical trials data management with ease and elegance. Clincase’s e-Clinical Technology Solutions offers access to an integrated set of features, services and added functionality all from one login. A seamless, versatile and robust EDC software, Clincase keeps data managers, monitors and sponsors connected to study performance and progress while encouraging increased site and investigator participation. Clincase provides easy-to-use, time-saving solutions that make data available in real-time. Clincase is a zero-footprint solution offered via secure, encrypted data transfer. Clinical trial data is hosted in a secure environment in Germany that upholds the highest standards of physical security. Our system is fully redundant, meaning data is constantly mirrored to a secondary data center for assurance, and full backups are created every day. -
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Seralogix Study Manager
Seralogix
An integrated suite of professional products, enabling you to dynamically share pre-clinical study data across an enterprise and around the world, with cutting-edge functionality, and industry-embraced standards. Seralogix Study Manager™ is a new platform aiming to standardize and streamline pre-clinical studies via an elegant interface. Suitable for individual researchers and scalable to vast research enterprise, the platform employs sophisticated computing power to make your experimental design, data collection, and reporting a breeze. This suite of tools will enable you and your team to have confidence in your data quality and enjoy the benefits of instant reporting. Correctly planning your experimental design can be a daunting task. Seralogix Study Manager walks you through the process of experimental design to achieve the statistically rigor necessary to ensure your studies success. -
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GraphPad Prism
GraphPad Software
A versatile statistics tool purpose-built for scientists-not statisticians. Get a head start by entering data into tables that are structured for scientific research and guide you to statistical analyses that streamline your research workflow. No coding required. Gain insights and guidance at every step so you make the right analysis choices, understand the underlying assumptions, and accurately interpret your data along the way. Prism makes it easy to collaborate with colleagues, receive feedback from peers, and share your research with the world. Go from data to elegant, publication-quality graphs-with ease. Prism offers countless ways to customize your graphs, from color schemes to how you organize data. Export into almost any format, send to PowerPoint, or email directly from the application. Master the art and science of data analysis and visualization through exclusive learning materials developed by highly-technical experts. -
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Protocol First
Protocol First
Protocol First not only bridges physical distance and breaks down the silos in Clinical Research during the pandemic, but our solutions are also suited to “normal times”. Technology that was once nice-to-have, is now a necessity. We provide the tools to stay connected, and not just to continue your research, but accelerate it. A complete remote monitoring tool with auto-tagging capabilities. Works with any EDC, anywhere, anytime. Protocol First has focused on breaking down the silos between Sites, Sponsors, CROs and functional areas. We offer comprehensive solutions to address the many dysfunctions of Clinical Research. Protocol First is built around getting your data right and in the right places. Today and in the future that includes AI/NLP/ML. The most important aspect to AI is making sure your data has an underlying structure. The family of software at Protocol First ensures that your data from patient to FDA is able to leverage the power of data science. -
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AQ2 Remittance
AQ2 Technologies
Any company that accepts checks as a form of payment can benefit from AQ2 Remittance. AQ2 Remittance is scalable for businesses that process as few as 25 to 50 checks per day, up to hundreds or even thousands of checks daily. Using check capture technology, you can significantly reduce operations and labor costs. AQ2 Remittance allows users to electronically transmit check images and related information quickly, without relying on couriers or daily trips to the nearest branch. Furthermore, the high costs of manually listing check amounts on deposit slips, manual research processes, and hardcopy distribution all become things of the past. A full featured check capture and electronic deposit solution for businesses. Capture data for uploading into your accounts receivable system. -
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DiData
DiData
DiData offers a versatile web-based software solution for clinical researchers, medical laboratories and hospitals that is customizable depending on the clients' needs, currently, its current main uses could be split into 3 categories : -Laboratory stock management software (Di-Freeze). -Electronic Data Capture System (Di-EDC). -Laboratory Information Management System (Di-Lims). Some of its features : - Blazing fast rendering with proven usability on large data sets. - Fast deployment : Easily integrate with your current systems/instruments thanks to available libraries and REST-API - Data view features : Use filters, Edit columns and Highlighter to make the best view of your data. - Dashboard : A fully customized module that enables you to shape it according to your needs. More main features and advantages are listed in-detail on our website.Starting Price: Varies -
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CSAM Registries
CSAM Health
CSAM’s Registries platform (previously MedSciNet Registries) provides a rich and versatile online environment for hosting registries, featuring powerful tools for all phases of the project’s life cycle, from data collection to analysis. CSAM’s Registries system design draws on our decade long experience of developing web-based software for medical research and offers a sophisticated online application package for hosting, maintaining, and monitoring registry projects of every size and scope. CSAM’s standard registry system implementation features a complete set of components required for setting up a fully functional registry. The system provides support for sophisticated data entry forms, flexible workflow structures, and advanced data validation, monitoring, and analysis. -
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Fusion eClinical Suite
Axiom Real-Time Metrics
Fusion is Axiom’s proprietary easy-to-use and cost-effective eClinical solution that is focused on small to medium sized device, pharma, and biotech companies. With Axiom’s Fusion eClinical Suite, you can add-on any Modules to meet your study requirements. Running a small study? Just choose the base configuration with EDC, DM and AE/SAE Tracking. Running something more complex? Include powerful Modules such as Inventory Tracking, RTSM, Safety Management to make the management of your study so much easier. Save time by capturing your study data electronically – even when offline! Data syncs to your Fusion databases once an internet connection is established. Access real-time records for Subject screening activities. Safety Database for the management of pharmacovigilance events directly within Fusion. -
48
naturalFORMS
ExpeData
Collect any type of form information such as calculations with validations to ensure complete and accurate results. Capture electronic signatures directly on the device or through the web. Signatures are secure and digitally certified. Snap photos for documents or attach images directly from the gallery. Photos can be annotated and included in a sketch. Create greater documents and photos by adding enhanced drawings, graphics and annotations. naturalForms integrates with hundreds of applications to allow you to eliminate manual processes and be super productive. Quickly enter information using the virtual keyboard, checkboxes, drop-down option lists, radio buttons, and date and time wheels. Set up mandatory fields or perform validation checks to ensure that incoming data is accurate and complete. -
49
Digitalis Clinical Data Collection
Cerebellis
Digitalis is an innovative data collection tool (Electronic Data Capture). Digitalis provides you with all the tools you need for a pleasant and complete collection and management of quality clinical data. It is a dynamic and ergonomic web application, whose strength lies in its ease of use and ability to adapt to your specific needs. Digitalis is a web-based software, which requires no special installation, a web browser and an internet connection are enough. The software is designed for the latest web browsers (Chrome, Firefox, Safari) but remains functional on older browsers such as Internet Explorer 9. Whether you work on your computer or on your tablet, Digitalis is used in the same way and adapts to the size of your screen. Thus, you can use the application from your tablet effortlessly using a thoughtful interface designed for your device. -
50
Track.Health
Pryzm Health
Secure and user friendly cloud-based EDC platform for managing clinical trials and studies of all sizes and complexities: ePRO, eConsent, eCOA, eSource, PROMs, PREMs, functional health assessments and participant education/engagement.Starting Price: $1/participant/month