If you are looking for a comprehensive list of EDC Software Vendors, then you are in the right place.
At betterclinical we work diligently to try and categories the major variations of software and technologies used to run and manage clinical trials. In the case of EDC software vendors, we have identified over 50 EDC software solutions. We will update the list from time to time. However, visit the EDC software directory to view the most updated list.
Electronic Data Capture (EDC) software is used in clinical trials to digitally collect, validate, audit, manage, store and analyze clinical research trial data, ensuring real-time access to critical information. It replaces traditional paper-based methods, offering greater efficiency, accuracy, and compliance with regulatory requirements.
EDC software plays a pivotal role in clinical trial operations by streamlining the data collection process, allowing researchers to capture data directly from patients, clinical sites, and laboratories. This enhances data quality, reducing errors, accelerating trial timelines, ensuring data accuracy and ultimately enhancing regulatory compliance.
According to research reports, the EDC market is expected to show strong growth over the next decade. The continued growth of the global electronic data capture (EDC) market can be attributed to the growing number of clinical trials across the globe, the continued complexity of capturing and managing data before, during and after a clinical trial and the continued technology maturity of pharmaceutical companies and CROs to web-based applications.
For the sake of clarity, we have provided the list of EDC Software Vendors Solutions in alphabetical order and provided the description found on the vendor’s website.
This is not a review of each vendor’s solution. It is simply highlighting available EDC software solutions.
Product Summary
Advarra is an EDC Clinical Trial Vendor that quickly and easily captures data. The system ensures data security and integrity using audit trails and secure signatures to fully support 21 CFR Part 11 validation and compliance. Advarra offers services to assist validation and materials to ensure validation is maintained throughout each upgrade.
About the company
For over 35 years, Advarra has been dedicated to advancing clinical research. From our origins in ethical review, Advarra has grown to become the premier provider of institutional review board (IRB), institutional biosafety committee (IBC), data monitoring committee (DMC), endpoint adjudication committee (EAC), site and sponsor technology solutions, and research quality and compliance consulting services in North America with reach across the globe.
We believe that Advarra can make the most impact by offering integrated solutions across the clinical trial ecosystem. Over the years, we have thoughtfully added to our capabilities with additional products and services to make clinical research safer, smarter, and faster for sites and sponsors..
Product Summary
The most intuitive EDC Clinical Trial Vendor 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, therefore, resulting in faster study submission times.
About the company
Anju is a customer-first organization providing adaptable life science solutions for clinical research, medical affairs, and data science. TrialMaster, IRMS MAX, and TA Scan, the company’s flagship products, reduce complexities in the drug and device discovery and commercialization process allowing our customers to enhance the quality of their patients’ lives.
Product Summary
Axiom Fussion EDC Software
About the company
Axiom was founded in 2001 by Andrew Schachter and has steadily expanded since its inception. Profitable since its second year, Axiom has been smart about when and where it moved forward.
The company was launched with a focus on registries and working with global clients. By 2003, the technology had evolved to a full registry and EDC offering with clients from start-ups to big pharma. In 2006, the business was pivoted to focus exclusively on small-to-mid size life sciences companies on the leading edge of their disciplines, delivering powerful eClinical tools [EDC, DM, IWRS, Reporting] and Data Management professional services to meet their unique requirements.
Product Summary
Castor EDC software is designed with usability in-mind for all, regardless of technical expertise.
About the company
Founded in 2012, Castor enables researchers to easily capture and integrate high-quality data from any source on one compliant platform. Thousands of medical device, biotech, and academic researchers around the world are now using Castor’s eClinical solutions to accelerate their studies.
Castor currently employs more than 100 people that are passionate about transforming medical research across its headquarters in Amsterdam, the United States and remotely.
Product Summary
Using Captivate® EDC software, you receive the benefits of Private Clinical Cloud® while enjoying a sleek and modern user-interface. Captivate® offers privacy, performance, and power — the scalability to run studies of different complexities and budgets. Modules that can be added to any package: Captivate® Coder (Medical Coding), VDC® electronic Patient Reported Outcomes (ePRO), VDC® electronic Clinical Outcomes Assessment (eCOA), Captivate® Randomization and Trial Supply Management (RTSM).
About the company
Captivate® is a suite of eClinical applications built on ClinCapture ’s eSource Platform and powered by the Private Clinical Cloud®. The Captivate® Platform was developed specifically for clinical researchers, as it uniquely provides the privacy, performance, and power to meet regulatory requirements, facilitate trouble-free data entry, and allow researchers to gain insight into data in realtime.
Product Summary
Clincase is a powerful EDC and clinical data management solution that enhances control over the clinical trial process. It provides a comprehensive range of features and functionalities to streamline the collection and management of clinical trial data.
The Clinicase EDC system provides a comprehensive range of features and functionalities while seamlessly integrating ePRO questionnaires to streamline the collection and management of clinical trial data. Clincase keeps data managers, monitors, and sponsors connected to study performance and progress while encouraging increased study participants and site involvement.
About the company
Clincase is an end-to-end EDC and clinical data management system. It provides a complete and integrated environment for the implementation, testing, and conduct of clinical trials for CROs, biopharmaceutical, and medical device companies.
Clincase has almost 20 years of experience with EDC software. Our team has high expertise in Data-Management, Software Development, Clinical Research, Project Management, and Data Privacy.
Extensive Usage and Industry Adoption: Clincase is widely adopted in pharmaceutical and biotech industries, utilized in Phase I-IV trials. It’s used by organizations globally, including CROs, research centers, and university hospitals in Europe, the U.S., and Asia. It has been deployed in 400+ studies, documenting data for 100,000+ subjects.
Adaptation to Regulatory Landscape and Enhanced Data Collection: Clincase has adapted to evolving regulatory requirements, integrating advanced reporting and data visualization features. The added capabilities of Clincase empower users to implement strategic and risk-based approaches in their clinical trials.
Product Summary
About the company
CRFWEB by Clindox provides a clinical trial software that focuses on affordability and efficiency, using a digital approach to replace traditional paper-based methods. Clindox launched CRFWEB in 2015, aiming to simplify clinical trials for a wide range of organizations. The company has grown to serve multiple countries and industries, praised for its supportive team and integrated system features like randomization and kit management.
Product Summary
About the company
Founded in 2016, we specialize in developing and implementing robust technology solutions for Life Sciences R&D. We help Pharma, Biotech and CROs in Clinical trials by implementing innovative technologies that involve Data warehousing, Analytics, Collaboration, Automation, and Artificial Intelligence.
With our unique combination of domain experience & technology expertise, we are committed towards delivering the most efficient and the best practical end-to-end software solutions with HIPAA, GXP, CSV, 21 CFR Part 11 and other applicable regulatory guidelines.
Product Summary
Review, query and lock visits in real-time: Clinical monitors can perform full source data review, issue/close queries, and mark visits as reviewed. CRIO’s system solicits PI signatures contemporaneously, allowing the sponsor team to continuously lock visits, enabling faster data locks.
Perform medical coding: CRIO has built-in WHODrug and MEDDRA dictionaries, with coding and review workflows. Sponsors can even embed the medication list at point of capture to increase autocoding and accelerate the coding workflow!
Review uploaded site PDF files: Reviewer also lets the clinical team review uploaded PDFs, including executed CRIO eConsent forms and EMR records, plus any other files uploaded by research sites. Review, query and lock the files, just as with direct data capture.
About the Company
Founded in 2015, CRIO’s goal is to transform the clinical trial industry by reimagining workflows from a site-centric perspective. By automating protocols at the site level, CRIO’s technology builds quality at point of capture, unlocking significant downstream benefits for sites and sponsors alike.
Product Summary
Clinion EDC Software is an intuitive tool that simplifies Clinical data management and allows easier study setup, data capture, processing, and integration. Users can quickly build and manage studies on their own with our AI-enabled EDC Software.
About the company
At Clinion, our mission is to empower CROs and sponsors in achieving clinical trial success through innovative AI-powered eClinical solutions. We commit to reducing time to market and increasing ROI for our clients.
Product Summary
Form Builder: Allows users to create and customize electronic case report forms (eCRFs) for data collection. Protocol Management: Tools to define and manage study protocols, including visit schedules, inclusion/exclusion criteria, and randomization procedures. Workflow: Design study specifications independent or complex workflow. Scheduling: Allows to set up schedule of visits that comes in sequential manner, visit interval along with positive and negative deviations.
About the company
From decentralized trials to our clinical trial consulting services, our therapeutic, technical and functional team is underprop by the culture of ethics and patient safety. Our experts and developers can work on complex business challenges with your team to help you achieve your goals and define a roadmap of necessary changes, whether by implementing new solutions or transforming existing legacy processes.
Product Summary
CLIRINX EDC (Electronic Data Collection) provides a suite of software products to support web-based data collection on your clinical research study. Branching/skip rules can be implemented on individual questions, groups of questions and fields within table-based questions. And if you need a new feature or application, we can develop it for you!
About the company
We provide 21CFR11-compliant web-based tools that support research initiatives and accelerate the discovery of new cures and better treatments. Our tools include study management, electronic data collection, and a participant portal, among many other advanced IT solutions. We are dedicated to supporting internet-based research, team science, and disease advocacy groups. CLIRINX offers IT expertise and assistance with patient registries, natural history studies, clinical trial readiness studies and research studies. Our team of experts can provide support and guidance throughout the entire research process, from study design to study close-out.
Product Summary
Cloudbyz EDC is a user-friendly, cloud-based solution that is designed to capture 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.
Cloudbyz EDC enables rapid study build with point and click with an interface that helps users build forms and easily navigate to the appropriate screens for data collection and analysis.
About the company
Cloudbyz was launched with a vision to reinvent enterprise applications in the cloud for industry verticals. We also put aside 1% of our employee time and 1% of our product, as well as, invest in the communities where we work and live. Our employees are encouraged and enabled to have a positive social impact.
Product Summary
About the company
Crucial Data Solutions was founded in 2010 by a group of clinical technology experts to help drug and medical device companies get their products to market faster. By launching TrialKit, they created an alternative to high-cost, high-burden data collection and study management solutions on the market.
TrialKit was designed to address unmet needs for medtech, pharma and biotech sponsors and CROs looking for a more seamless, cost-effective solution.
To this day, Crucial Data Solutions remains laser-focused on its mission; to help our customers reclaim control and enhance the health and quality of life of their patients by delivering advanced, affordable clinical technology.
Product Summary
About the company
CRScube provides customizable and modular solutions designed to benefit clinical trials across all phases and therapeutic areas by automating processes, eliminating inefficiencies, and streamlining end-to-end operations.
Product Summary
Curebase is a clinical trial management platform that includes ePRO/eCOA, eConsent, telemedicine, payments, scheduling, and EDC. It is a suite of eClinical software solutions that can be used for designing, building, and executing studies, and to improve clinical trial recruitment, consent, and data collection. Curebase is intended to be user-friendly and can be used by CROs, sites, and participants.
About the company
At Curebase, our mission is to bring quality medical innovations to patients faster. We offer a full package clinical trial tools and services. All leading to to faster, cost effective, and diverse studies.
We are proving that clinical research can be radically accelerated if we empower physicians everywhere to enroll patients in the communities where they live. By applying cutting edge clinical software and remote study management techniques to the problem, we are reinventing clinical trials and research from the ground up.
Product Summary
Easily implement edit checks and visibility conditions, from simple to complex, without any coding skills. Validate data effortlessly cross forms/visits, reducing errors. Create professional studies quickly. Take advantage of templates, saving time and effort.
About the company
Streamline the management of your trial effortlessly with the Datacapt platform. Developed by specialists and experts, our platform is highly flexible and tailored to suit your specific studies. Enjoy the convenience of a modular platform that consolidates all the necessary elements in one place, enabling you to design and manage all aspects of your trials seamlessly (including EDC, eCRF, ePRO/eCOA/eDiary, eConsent, eConsult, and Data Analysis).
Product Summary
About the company
Founded in Seattle, DFnet seeks to provide accessible and efficient data analysis, data management, and data science resources focused on public health. With the combined skills of clinical researchers, data managers, and software developers, we embark on an important mission: supporting and improving pivotal research on a global scale.
Though we may have officially introduced ourselves as DFnet in 2004, our roots go much deeper. In fact, we’ve been around longer than electronic data capture itself — the “DF” in our name stands for “DataFax,” an homage to the fax machines we initially used for research. By bridging paper case report form and electronic data capture, we developed a strong background and a thorough understanding of the methods used to record global research. For over 30 years, we have brought experience and precision to clinical trials and studies.
Product Summary
Di-EDC is an Electronic Data Capture EDC system for clinical research Made by Researchers for Researchers. Using our intuitive interface to manage your Research Data and Projects in a compliant environment, becomes at the hand of all researcher
About the company
Founded by a team of visionary scientists and technology enthusiasts, Didata was born out of a passion for innovation and a deep understanding of the challenges laboratories face daily. At Didata, we collaborate with medical doctors and scientists, that’s what makes us the driving force behind the modernization and optimization of laboratory operations. Our commitment to empowering laboratories with cutting-edge technology has made us a trusted partner in the world of scientific research and data management.
Product Summary
Do you have a web browser? Perfect, you are ready.
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.
Computer, tablet … Digitalis adapts to the size of your screen.
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.
About the company
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.
Product Summary
About the company
Data Management 365 is a software firm with deep expertise in clinical trials. We emphasize robust skills in Clinical Data Management and Data Science, enabling us to address Data Managers’ challenges, enhance our MainEDC™ platform through real-time feedback, and share best practices with clients. This expertise also aids communication with Clinical Data Management professionals. We originated as a spin-off from Flex Databases and were founded by IT experts, doctors, and researchers experienced in clinical trials. Thus, we intimately understand and cater to Data Management Software needs using cutting-edge tech.
Product Summary
Secure clean data
The most successful decentralized or traditional clinical trials begin and end with the highest quality, clean data. Electronic Data Capture (EDC) software is a computerized system designed for the collection of trial data in a electronic format or eCRF that is used in human clinical trials for FDA submission. The most efficient and streamlined way to collect and capture clean clinical trial data is only accomplished when using the best clinical trial software in the industry, eCaseLink.
Simple cost-effective integration
The most experienced eClinical provider in the industry, eCaseLink provides study managers and users with intuitive, simple-to-use tools without the need for any programming knowledge. This ensures that any clinical trial is easy, streamlined and best of all, cost-effective.
Speed, efficiency and accuracy
eCaseLink not only meets these critical needs but goes above and beyond to become your ultimate tool for clinical trial success. Our integrated unified software platform enables you to manage your clinical trial life cycle with just one solution provider or gives you the option to “plug and play” with multiple components, giving you flexibility and choice not seen anywhere else.
About the company
With over 30 years of eClinical experience our roots run deep within the clinical trial study and life sciences industries. Since our founding in 1992, DSG has produced the most innovative software solutions for the pharmaceutical, medical device and life sciences industries world-wide.
DSG’s clinical trial software and data management services have grown over the years because of our understanding of new technologies and our collaborative approach with our clients. In our beginning, and before the internet became mainstream, DSG pioneered CRF document management software, setting an industry standard. Our best-of-breed eCaseLink allowed individuals to build CRFs electronically, greatly reducing the amount of time it takes to run a clinical trial. eCaseLink became the industry standard, and has been trusted and utilized world-wide by the top 5 pharmaceutical companies since 1992.
Product Summary
Simplify Clinical Data Collection with Ennov EDC. Configurable edit checks, allowable values library, and pre-integrated with eTMF and CTMS..
About the company
One of the fastest growing clinical trial solution providers, with a vision and mission to change the future of clinical trials by bringing innovations through our digital platforms leveraging real-world insights.
From decentralized trials to our clinical trial consulting services, our therapeutic, technical and functional team is underprop by the culture of ethics and patient safety. Our strong conviction and commitment is to our clients in bringing the next generation quality therapies faster to the market.
Our experts and developers can work on complex business challenges with your team to help you achieve your goals and define a roadmap of necessary changes, whether by implementing new solutions or transforming existing legacy processesHeadquartered in Paris, with offices in the US, UK, and Asia, Ennov provides the most original, comprehensive and cost-effective suite of software solutions for the Life Sciences industry. From leading pharmaceutical companies to emerging biotechs, we proudly serve over 250 companies and 250,000 users around the world.
For more than 20 years, we have been developing innovative, powerful and easy-to-use software for regulated content, data and process management. Our solutions are designed and built to support the entire Life Sciences R&D continuum including Clinical, Regulatory, Quality, Pharmacovigilance and Commercial. Ennov is ISO9001:2015 certified for all software products and processes and we boast a 100% success rate in customer audits.
We are recognized by Gartner as a global provider of software technology for the Life Sciences in the areas of Enterprise Document Management (EDM), Regulatory Information Management (RIM), Pharmacovigilance, and Electronic Trial Master Files (eTMF) – a testament to our focus and innovation.
Our solutions enjoy extremely high user adoption rates, thanks to our intuitive user interfaces and commitment to building solutions that work the way our users work. We also have very high customer satisfaction ratings with an on-time project delivery rate of 98.5% and an annual maintenance renewal rate of 96%.
Product Summary
We provide a flexible software that enables easy study set-up and management. Customers and end users value the simplicity of customizable workflows. According to our clients, one of the key advantages of using our system compared to other EDC tools, is its quick implementation. A study set-up is possible in weeks not months.
About the company
We launched Cloudbyz with a vision to reinvent enterprise applications in the cloud for industry verticals. We put our customers and partners first and make them wildly successful with our innovative cloud apps and solutions. Our deep expertise in the industries we serve and ensure that our products and services delight our customers and transform their organizations.
Leveraging more than 50 years of combined experience in providing innovative and creative ways to conduct clinical trials we have achieved:
Product Summary
About the company
Flex Databases was founded in 2011 and to this day remains privately owned by our working managers. Our HQ is in Prague, Czech Republic, with additional offices in Switzerland, the U.S., and Turkey. Our clients are based all over the globe. About half are CROs, and half are sponsors including pharma companies, biotech, medical devices, and academic research.
Now, you are probably wondering about security, compliance, and validation. We provide truly comprehensive service, taking care of system roll out, implementation, data hosting, backups, security, as well as validation and compliance. We are GCP, GMP, HIPAA, GDPR compliant, have participated in numerous audits, and experienced helping clients during inspections.
Product Summary
Global Vision ClinicalPURSUIT is a clinical electronic data capture software. It enables you to rapidly set up and deploy single-center and multicenter studies in weeks. Its clinical trial data management services offer advanced user management and streamlined workflow to effective data capture for all your clinical trials.
ClinicalPURSUIT’s powerful clinical data EDC system tools allow you to easily keep a pulse on your clinical trial data status and quickly act when needed. Our configurable dashboards deliver exactly the information you need – whether you are a study sponsor, a CRO, or a clinical data manager.
About the Company
Global Vision Technologies transforms casework and client management. Our systems streamline data capture and simplify tedious or time-consuming workflow. Subject matter experts, social workers and technologists are proven integration specialists; they’ve been where you are and have critical insight on leveraging best practices to make your implementation a rewarding experience. Our data scientists know how to present your data quickly, when you need it the most – so your decisions are made faster. In short… we protect you.
Product Summary
Ensure compliance from the start with built-in ISO 14155:2020, EU MDR, and FDA requirements. In addition, you’ll get 13 ready-to-use and customizable compliance document templates.
Support for multi-indication device studies.
Easily make adjustments to your study designs according to different countries’ requirements and EC approvals.
Support for dynamic visits and treatments.
If your study subjects require one or many treatments with your device, you can use multiple activations for any visit event.
About the company
In 2006, Jon Speer, a medical device engineer turned consultant, had the initial idea for Greenlight Guru, when he made a simple observation: paper-based quality management systems (QMS) are painful, risky, and inefficient. At the time, commercial QMS solutions had been available for nearly two decades, but only 30% of MedTech companies were actually using them. This observation led Jon and his co-founder, David DeRam, to develop Greenlight Guru. Today, with our powerful, intuitive solution, MedTech companies across the world can bring higher quality, life-changing products to market faster, more efficiently, and with less risk.
Product Summary
ICON Prism Connect extracts clinical trial information directly from a site’s electronic health records (EHR).
Key benefits
Cost savings: By eliminating the need to enter the same data in multiple systems, Prism Connect increases efficiency and saves cost.
Process efficiencies: The sponsor receives the data faster, leading to accelerated delivery of novel therapies to patients.
Cleaner data: The data is cleaner as many of the data points are migrated directly from the source (EHR).
About the company
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.
Product Summary
Real-time Data Access
Intelligent query management allows you to access data in real-time, which also facilitates faster analysis
Powerful Visualization
Build easily understandable reports with attractive visuals like bar charts, line graphs, and scattering plots
Schedule Tracking Events
Set event-based or time-based schedules to trigger alerts and send notifications to concerned stakeholders
About the company
We are a team of 120 + passionate workforce that carry a unified client centricity focus day in day out. The combined 500 + years of niche skills experience is the founding strength of our company.
We built a team who are not just experts but also empathetic towards making a difference in the world. Our mission is to use emerging technologies like AI/ML, data analytics and deep learning to help our life sciences and healthcare partners with transformative and reliable results.
Product Summary
Our EDC software of the eClinical cloud allows you to electronically capture clinical trial data with confidence, in the proper format, with edit checks and validation to ensure a successful clinical trial.
This is done using their innovative one-login unified software platform for end-to-end study execution. The Jeeva platform eliminates the need for numerous point solutions and vendors. This helps boost efficiency for all users. The platforms also includes:
About the company
After suffering the loss of a child to a rare congenital disorder and a brother to a chronic disease, Jeeva founder and CEO Dr. Harsha Rajasimha decided to apply his years of postdoctoral training at the National Institutes of Health and the U.S. Food and Drug Administration. His work in the healthcare and life science industry focused on accelerating access to treatments for rare & chronic diseases by eliminating bottlenecks in the clinical trials process.
Product Summary
Hyper Connectivity: Integration with third party solutions for the most optimal data management·
Seamless Journey: Modular structure allows full customization to fit all clinical trial designs·
Data Secured: Tamper-free data protected by blockchain-based audit trail
About the company
One of the fastest growing clinical trial solution providers, with a vision and mission to change the future of clinical trials by bringing innovations through our digital platforms leveraging real-world insights.
From decentralized trials to our clinical trial consulting services, our therapeutic, technical and functional team is underprop by the culture of ethics and patient safety. Our strong conviction and commitment is to our clients in bringing the next generation quality therapies faster to the market.
Our experts can work on complex business challenges with your team to help define a roadmap of necessary changes, whether by implementing new solutions or transforming existing legacy processes. JNPMEDI was established to advance the internationally recognized Korean medical infrastructure by offering clinical trial solutions of the highest data integrity and operational efficiency.
Product Summary
• 12 drag and drop form field options
• Start with a study template
• Set min and max limits for each form field
• Skip future questions based on the answer to a previous question
• Weight questions and calculate scores for completed surveys
About the company
Our mission is to accelerate regulated digital health innovation for our biopharma and medtech customers through our scalable medical-grade platform. Whether you’re developing a companion app to improve adherence, adding connectivity to a medical device, or deploying a smart algorithm that can personalize patient care in real-time; our software and services take the hard work out of building, scaling and maintaining digital health offerings.
Product Summary
Make Data Entry Easier and Faster For Your Sites
Rave Companion reduces clinical trial data entry efforts for sites by making it simpler and faster to get source data from any system (e.g., EHR – electronic health record) or document (e.g., lab values in a spreadsheet) into Rave EDC.
Centralized Administration and Master DataExpand
Real-time Data ValidationExpand
Patient Data SurveillanceExpand
Reporting and Analytics
About the company
Medidata is leading the digital transformation of clinical research, creating hope for millions of patients. Our unified platform combines AI powered insights with unrivaled patient-centric clinical trial solutions to help pharmaceutical, biotech, medical device and diagnostics companies, as well as academic researchers accelerate value, minimize risk, and optimize outcomes.
Medidata is the first life sciences tech company to surpass 30,000 trials and 9 million participants. We’re powering smarter treatments and healthier people, with over 1.5 million registered users across 2,000+ customers and partners harnessing the world’s most trusted clinical trials software for clinical development, commercial, and real-world data.
Product Summary
Most researchers and analysts are perfectly able to analyze a dataset using tools such as Excel, SPSS, SAS, R etc. It becomes much more challenging when you want to harmonize your data across different data sets. Or want to work consistently with standardized terminologies or data dictionaries.
MediGrid has a smart data ingestion engine that not only structures your data well and helps to curate your data, it is also able to transform and harmonize your data. This allows researchers to conduct multi-study analyses or to review adverse effects across multiple studies for example.
About the company
MediGrid was founded in 2020, the year the world faced a pandemic that resulted in a global health and economic crisis. Not only did COVID-19 put a major stress on the entire health system, it also created a major task for the academic and pharmaceutical industry: find proper treatments and a vaccine within months instead of years.
Product Summary
Make Data Entry Easier and Faster For Your Sites
iMednet’s Core EDC Features:
About the company
Mednet is a leading healthcare technology company specializing in eClinical solutions designed for the global life sciences community.
With more than two decades of experience and thousands of studies conducted with both CROs and life sciences sponsors, we have the knowledge and experience to help you achieve success. From our Leadership to our Board of Directors to our product development experts and professional services teams, Mednet has the real-world experience to effectively support your clinical research projects from start to finish.
Our EDC-centric eClinical platform, iMednet, optimizes clinical studies of all types and sizes, across all therapeutic areas – accelerating research with exceptional flexibility, ease-of-use, robust functionality, affordability, and stellar support. Learn more about our strengths
Product Summary
Zelta’s electronic data capture system is a flexible and secure eClinical solution. Used in more than 4,000 studies from startup to submission, across all phases, including over 500 phase III trials and 23 therapeutic areas, Zelta makes it easier to execute the complex.
About the company
Merative is founded as a data and analytics partner for the health industry. With an essential combination of trusted technology and human expertise, Merative drives shared progress by putting people at the center of health.
Product Summary
Quick and clear overview of patient data at all times.
Robust data validation checks and automatic calculations
Generate compliant, near submission-ready data; thus, facilitating faster submission of study results for regulatory approval.
About the company
Octalsoft is a market leader in the field of eclinical solutions, IT consulting, custom software development, app development, digital transformation, and technology consulting. Established in 2007, Octalsoft sports over a decade of experience and a team of 60+ experts who have delivered consistent success with over 30000 platform users and a clientele spread across 22 countries. Here is glimpse of how we reached where we are today.
Product Summary
True flexibility: 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.
Fast start-up: EDC system OnlineCRF is ready to go within 4 weeks (from approved Protocol and CRF). Send a request, and you will get feedback in 8 working hours. Check our speed right now.
Data safety: 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.
Saving your time: 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.
About the company
OnlineCRF is a vendor of EDC systems for conducting clinical trials.
Our experience of the actual clinical trials and postmarketing studies have given us a clear understanding of the needs of CRO and pharmaceutical companies in clinical data collection.
Among other things, we saw that small companies do not always have the ability to maintain a Data Management department. Therefore, we created an EDC system that is fully configurable for the client by our Data Managers. There is no need to hire data managers or outsource EDC configuration to other companies. You will get ready-to-go EDC, which is completely configured in strict accordance with the study protocol. Just log in and manage your clinical study.
An all-in-one solution gives you an easy, fast, and cost-efficient way to perform clinical data collection.
Product Summary
Update your forms as needed: the study build system will track versioning for you.
Preview the forms exactly how they’ll appear and function for your users from within the build system.
Publish to a test or production environment in less than a minute.
Invite study managers and sites with permissions you control.
Create a site or user once, and the system stores the record for use in other studies.
About the company
For over 15 years, OpenClinica has hired the best and brightest people to ensure that your clinical trial software solutions are of the highest quality. Nearly all of our employees have experience in the healthcare and clinical industries. We understand your challenges and make it our mission to mitigate those pain points so that you can get back to focusing on patients and advancing clinical research.
Product Summary
Oracle Life Sciences Data Management Workbench is the only clinical trial data management solution that provides a validated, trustworthy single source of truth for all trial data that automatically reconciles data discrepancies and provides complete traceability. You’ll know immediately when something is going wrong with a trial and be able to take action.
Get real-time access to trustworthy clinical trial data
Oracle Health Sciences Data Management Workbench gives you a complete, real-time picture of clinical trial data, providing visibility into the trial so that you can make better decisions quickly, effectively, and easily.
About the company
We’re a cloud technology company that provides organizations around the world with computing infrastructure and software to help them innovate, unlock efficiencies and become more effective. We also created the world’s first – and only – autonomous database to help organize and secure our customers’ data.
Oracle Cloud Infrastructure offers higher performance, security, and cost savings. It is designed so businesses can move workloads easily from on-premises systems to the cloud, and between cloud and on-premises and other clouds. Oracle Cloud applications provide business leaders with modern applications that help them innovate, attain sustainable growth, and become more resilient.
Product Summary
Build User-Friendly Workflows
• Allow users to access your study from anywhere in the world at any time
• Control access to every aspect of your study, including masked and blinded data points
• Follow your sites’ progress by tracking study participation and performance
About the company
Founded in 2003, our founders created Prelude from the ground up as a new type of electronic data capture (EDC) system – that is, with the end-user in mind while still being able to withstand the most extreme scrutiny for data, accuracy, and speed.
Product Summary
Accelerate your research with the QuesGen EDC platform. Once funded, most studies need to be set up quickly and enrolling participants becomes a priority. With QuesGen’s fast study building capabilities, studies can be set up and begin screening participants within just a few days.
With the QuesGen platform, your study will have established standards and processes. This will help to maximize the use (and re-use) of the your data collection efforts, creating standard practices and forms as well as applying common project management principles.
About the company
QuesGen is a Brain Health CRO uniquely developed for academic and commercial research studies and clinical trials. QuesGen was founded in January 2004 with the vision of providing an easy to use web-based general use data management platform primarily for academic use. Over the last 15 years, QuesGen has grown into a full-service CRO company focusing on Brain Health. Though we still work in all areas of research, we have particular expertise in Brain Health and TBI research. Our focus on Brain Health began with a study out of UCSF called TRACK Pilot. The pilot began in 2009 and is now known as TRACK-TBI.
Since that initial project, we’ve added many additional TBI research projects including CENTER-TBI and The NCAA/DOD funded CARE Consortium. Although the QuesGen software is a general use software platform, our experience in brain research has allowed us to accumulate an extensive library of off the shelf outcomes and assessments allowing for rapid study deployment. Additionally, our work in this area of brain health research has given us a unique perspective on which outcomes and assessments work best in which situation.
Product Summary
• CUSTOMIZE
• Build custom eSOURCE documents to standardize processes and workflows.
• COLLABORATE
• Create reminders for doctors and staff to take action.
About the company
Quad One is a Life Sciences Technology company. Our clinical trial solution, Clinion, is an all-in-one AI-enabled eClinical platform for clinical trial setup and management. Providing an integrated bundle of EDC, CTMS, IWRS/RTSM, eCOA, Document Automation.
At Clinion, our mission is to empower CROs and sponsors in achieving clinical trial success through innovative AI-powered eClinical solutions. We are committed to reducing time to market and increasing ROI for our clients. By consistently delivering timely solutions, prioritizing transparent communication, and providing exceptional customer support, we aim to drive positive change in the industry and make a lasting impact on the world.RealTime Software Solutions, LLC is a leader in cloud-based software solutions for the clinical research industry and is dedicated to solving problems and providing systems that make the research process more efficient and more profitable. We are constantly listening to our customers and to the needs of the industry to provide new innovations that streamline processes and help us all achieve our operational goals. RealTime’s focus on exceptional customer service ensures that all clients get the most out their RealTime solutions!
Product Summary
• Manage studies of any size, complexity, or therapeutic area within a single, unified platform
• Deliver cross-functional and cross-study insights with a standards-based approach to data management and analytics
• Accelerate decision making through direct access to study data and real-time dashboards via our web-based portal or mobile EDC app
• Streamline study timelines by making design changes to active studies easily without the need for migrations
About the company
One of the fastest growing clinical trial solution providers, with a vision and mission to change the future of clinical trials by bringing innovations through our digital platforms leveraging real-world insights.
From decentralized trials to our clinical trial consulting services, our therapeutic, technical and functional team is underprop by the culture of ethics and patient safety.
REDCap Cloud powers data-driven digital research to accelerate medical discoveries, connect research and care, and establish new standards of scientific innovation based on real-world evidence. Our clients include enterprise and emerging biopharma, medical device companies, hospitals, and health systems around the world.
Product Summary
Online or offline project design
Online using the Online Designer or offline using a “data dictionary” template in Microsoft Excel that can be uploaded later into REDCap.
Availability
Software is available at no cost for REDCap Consortium Partners.
Secure and web-based
Input data or build an online survey or database from anywhere in the world over a secure web connection with authentication and data logging.
About the company
REDCap was created in 2004 at Vanderbilt University. It originally supported a small group of clinical researchers who needed a secure data collection tool that met HIPAA compliance standards. REDCap quickly became their go-to method for supporting both single and multi-site research studies.
REDCap’s developers firmly believed that nobody could know the research as well as the researcher. So a user-friendly web-based interface was introduced to put the researchers in total control of their work. No background knowledge or technical experience was needed to use REDCap; researchers could directly manage their own projects whenever and however they wished, through any browser on any device.
Product Summary
Trial Online EDC is designed specifically for the needs of extensive clinical trials. It is a robust and secure while still intuitive system that accelerates clinical study setup and data collection. It allows clinical study teams to configure trials effortlessly through an intuitive front-end trial builder, including role-based access, edit check validators, skip/add logic, derived calculations, among other.
About the company
Founded at the turn of the millennium, Replior began as provider of IT operation services for the Life Science industry.
Over the years, we’ve evolved, acquiring the Trial Online EDC software system in 2010 and setting out on a mission to become a trusted partner for data collection in clinical trials.
Our journey has been marked by collaboration, innovation, and a commitment to advancing patient care and research.
Product Summary
ResearchManager EDC provides an innovative alternative to data collection by replacing traditional (paper-based) methods with an electronic Case Report Form (eCRF). With EDC, we simplify and expedite the data collection process. Additionally, we reduce manual errors, enhance data entry, validation, and reporting efficiency.
About the company
More than 10 year in biomedical research
Our team consists of professionals with more than 10 years of experience in supporting clinical research and software development.
Our product automates the research processes, users manage it and monitor its progress online. We configure and validate the software before release that guarantees secure storage and data integrity.
Chronicles Research Team is a provider of software products for the GxP industry, which makes clinical systems available for small and medium-sized businesses.We empower researchers, patients, healthcare providers, and other stakeholders in clinical research. With our robust and modern Clinical Research Suite, we expedite the complete research process. We focus on digitizing the process for shorter study durations, digitizing data and information, as well as enhancing transparency and safety.
Product Summary
secuTrial EDC is a professional, entirely browser-based GCP-compliant EDC system. In addition to data capture using electronic case report forms (eCRF), secuTrial® offers users the facility to create their own eCRFs without any programming knowledge. The query workflow is also conducted completely via the Internet. As the data is checked for completeness and plausibility during the data entry stage, queries can often be avoided. In addition to eliminating errors caused by illegible handwriting, the quickly available reports make it easy to maintain a clear overview of the trial.
About the company
secuTrial® is a professional, entirely browser-based GCP-compliant EDC system for collecting patient data in clinical or non-interventional studies and patient registries.
Since the year 2000, secuTrial® has been used in over 600 national and international studies and long-term projects conducted by university institutions, CROs, med-tech manufacturers and pharmaceutical companies – a clear testimony to its superior product quality, universal applications and high customer satisfaction.
Product Summary
Achieve high-quality data with our EDC: dynamic validation ensures real-time consistency, automated reminders boost user engagement and data accuracy, and our flexible monitoring system allows you to tailor data review workflows to the needs of each study.
Improve control over your clinical trial with customizable notifications that allow you to stay informed of key events. Our reporting module provides intuitive visualizations of key metrics, allowing you to make data-driven decisions for better outcomes in your clinical trials.
About the company
ShareCRF is an electronic data capture (EDC) service for collecting and managing multi-site clinical trial and registry data.
Product Summary
About the company
Quad One is a Life Sciences Technology company. Our clinical trial solution, Clinion, is an all-in-one AI-enabled eClinical platform for clinical trial setup and management. Providing an integrated bundle of EDC, CTMS, IWRS/RTSM, eCOA, Document Automation.
At Clinion, our mission is to empower CROs and sponsors in achieving clinical trial success through innovative AI-powered eClinical solutions. We are committed to reducing time to market and increasing ROI for our clients. By consistently delivering timely solutions, prioritizing transparent communication, and providing exceptional customer support, we aim to drive positive change in the industry and make a lasting impact on the world.Today, Sitero is a next-generation clinical trial solutions partner, working with more than 200 Pharmaceutical, Biotech, and Institutional Research Organizations globally. Sitero uses technology to drive safety, compliance, quality, and efficiency in research and clinical trials, so customers can bring life-changing treatments to market safer and faster.
With leaders in Technology, Clinical Operations, Biosafety, Drug Safety, Ethical Review / IRB, and more, Sitero draws on a deep well of knowledge to build solutions for customers. As a technology and service-oriented partner, Sitero focuses on forging strong relationships that can drive efficiency by leveraging next-generation software.
Product Summary
About the company
One of the fastest growing clinical trial solution providers. From decentralized trials to our clinical trial consulting services, our therapeutic, technical and functional team is underprop by the culture of ethics and patient safety. Our strong conviction and commitment is to our clients in bringing the next generation quality therapies faster to the market.
Our experts and developers can work on complex business challenges with your team to help you achieve your goals and define a roadmap of necessary changes. Be it by implementing new solutions or transforming existing legacy processes. Sofpromed is a full-service Clinical Research Organization (CRO) specialized in the management of phase I-IV clinical trials worldwide for biotechnology and pharmaceutical companies across all therapeutic areas.
We manage clinical trials globally in the United States, United Kingdom, Europe, and Australia. In the EU we operate in key countries like Spain, France, Germany, Italy, the Netherlands, Poland, Czech Republic, Slovakia, Greece, and Georgia.
Product Summary
Our innovative Electronic Data Capture (EDC) tool with its agile methodologies allows users to set up and configure study databases in no time. Users can also design Case Report Forms (CRFs) with programmed edit checks and collect high-quality, accurate clinical data along with extracting submission-ready standardized datasets from an easy-to-use web-based graphical user interface.
About the company
At SyMetric, we help you make the shift from traditional trial models to agile, patient-centric processes driven by our unified Clinical Trial Platform. With us, you can use the power of technology to automate and simplify project management in clinical trials and improve your productivity. We offer modularized solutions for Pharma Companies, Contract Research Organizations, and Academia.
Product Summary
Features AI-powered functions that can parse word descriptions in trial protocols and convert them into eCRF structures for data collection in real-time.
Allows users to visualize data collected in a clinical trial by converting them into graphic reports, supporting all analytical and statistical needs from all roles.
The matrix design shows a clear layout for users to assign forms to visits, as well as manage eCRF versions by transferring collected data to new eCRF versions.
Can automatically test if all edit checks will run as expected with simulated data entry and generate a test report.
About the company
Founded more than 10 years ago, Taimei Technology has been offering clinical technology solutions for thousands of sponsors and hundreds of clinical service providers and has empowered over 7,000 clinical trials. Our global market coverage in North America, Asia Pacific, and Europe and database integration capabilities with regulatory agencies in more than 30 countries are a testament to our commitment to providing comprehensive solutions to our clients.
Product Summary
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..
About the company
TrialStat® delivers data solutions on-demand for pharmaceutical, biotechnology, medical device companies, Contract Research Organizations and Data Management companies. Our TrialStat eClinical Suite™ consists of three fully unified product offerings – EDC, Portal and CTMS. We stand alone in the industry with such an all-compassing suite of products for conducting clinical trials.
Product Summary
Vault Electronic Data Capture (EDC) provides an end-to-end environment to collect, review, and process trial data about patients.
During study start, Vault EDC is used to design patient forms (including edit checks) without the need for custom programming.
During study execution, Vault EDC collects all patient form data, local labs, and medical coding. It also has quality controls including querying, targeted source data verification (SDV), and protocol deviations. When protocol amendments happen, the Vault EDC database needs no downtime.
At the end of the study, Vault EDC provides data lock and post-processing features, including end-of-study media creation and archiving..
About the company
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 875 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Canada, Europe, Asia, and Latin America.
Product Summary
About the company
For two decades, we have perfected the craft of making clinical data more accessible so that greater discoveries can happen sooner. At Viedoc, 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.
