Alternatives to ResearchGuru EDC
Compare ResearchGuru EDC alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to ResearchGuru EDC in 2026. Compare features, ratings, user reviews, pricing, and more from ResearchGuru EDC competitors and alternatives in order to make an informed decision for your business.
-
1
ShareCRF
ShareCRF
Create, in a few hours, an eCRF that is as easy to use as a paper one, and avoid the biggest headaches in data collection in Pre-authorisation and Post-authorisation studies of your medical device. Incorporate an EDC that is highly flexible when creating the eCRF, this will allow you to meet the needs of any kind of study. Save tons of time in the management and monitoring of the study with the management and monitoring tools included in the EDC. Use a validated system with all the security guarantees that give trust to the sponsor and allow the collection of quality data. Don’t wait until the analysis phase to discover mistakes in the data or you will end up chasing down investigators to correct them. Prevent the process of creation of an eCRF from being long and complex.Starting Price: $500/month -
2
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. -
3
OpenClinica
OpenClinica
OpenClinica is a leading provider of clinical trial technology, offering a comprehensive suite of solutions to enhance the efficiency and effectiveness of clinical research. The platform provides electronic data capture (EDC), patient recruitment, eConsent, and clinical data management solutions, all designed to streamline workflows and improve data quality. OpenClinica also integrates EHR-to-EDC connectivity, allowing for seamless data acquisition and reducing errors. Trusted by life sciences companies, academic institutions, and government agencies, OpenClinica supports over 15,000 studies and has helped manage data for more than three million patients worldwide. -
4
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). -
5
Greenlight Guru Clinical
Greenlight Guru
Greenlight Guru Clinical is the only electronic data capture (EDC) system built specifically for medical device and diagnostics companies, not adapted from pharma. Designed exclusively for medtech, it combines an easy to use clinical data platform with industry leading customer service, helping teams generate reliable, compliant clinical data under FDA, EU MDR, IVDR, and ISO 14155 requirements. Get a single, validated platform for medical device studies, including: Electronic Data Collection and eCRF ePRO/eCOA (electronic patient and clinician reported outcomes) eConsent Randomization (RTSM) PMCF Surveys (post market clinical follow up) Adverse Events Reporting Open API Used by device manufacturers and medtech CROs running clinical investigations, PMCF studies, registries, and human factors testing. Every customer gets a dedicated customer success manager with real medtech experience and a validation package included with every product update. -
6
TrialKit
Crucial Data Solutions
TrialKit is a unified eClinical platform for sponsors, CROs, and research institutions, combining EDC, ePRO/eCOA, eSource, eConsent, RTSM, eTMF, medical coding, imaging, and more in one environment. Floyd, TrialKit's AI model, works directly within the platform to support protocol interpretation, study building, validation, simulation, and analysis. It can generate eCRFs, visit schedules, edit checks, and workflows, while synthetic participants help teams test study configurations. Researchers retain control over reviewing and refining study designs. Web and native mobile apps support data collection across traditional, hybrid, and decentralized studies. Open REST APIs enable integration with external systems, while audit trails and role-based access support study oversight. TrialKit also offers predictable monthly platform pricing without incremental change-order fees for routine study modifications. -
7
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. -
8
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 -
9
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. -
10
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. -
11
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 -
12
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 -
13
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 -
14
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. -
15
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 -
16
DADOS
DADOS
Our application provides a web-based interface to be used for collecting data from a variety of study types or clinical situations. With the built-in flexibility of its easy-to-use data capture methods to collect patient outcomes, data can be designed around any specialty, patient population, or research study. Improving the quality of care by tracking patient-reported outcomes and using population analytics. With a secure web-based interface, it is compatible with personal computers and tablets for data entry. Reports can be generated in real-time, allowing researchers to manage the entire process for single and multi-center studies, regardless of geographic location. DADOS Platform brings a top-notch user interface (UI) and do-it-yourself easy-to-use tools for clinicians and researchers to create programs or studies to bridge the gap between research and clinical care. Patients enjoy using DADOS because of its ease of use and availability anywhere. -
17
LabRelations
LabRelations
LabRelations is a modern, configurable laboratory platform built to centralize and streamline scientific and test workflows by combining core modules, including LIMS (Laboratory Information Management System), ELN (Electronic Lab Notebook), CTMS (Clinical Trial Management System) and EDC (Electronic Data Capture), into a single system that supports everything from sample tracking and experiment documentation to study management and regulatory-grade reporting while reducing manual work, errors and data silos; it lets labs store all data in one place, define rule-based workflows and automations, connect instruments and external systems, enforce full audit trails and compliance (such as GxP, 21 CFR and versioned controls), and configure objects, forms, views and permissions to fit specific lab needs, while enabling cross-functional collaboration and real-time visibility from discovery and quality control to clinical research and complex regulated environments. -
18
CORE (Clinical On-demand Research)
CIRU, University of Southampton
CORE (Clinical On-demand Research) covers a range of expert services which include the design, build and running of electronic forms used in clinical trials across the UK and overseas. Not only does CORE create the forms you need, it also offers randomization, data management and provides you with those all-important study statistics. CORE captures vital data for researchers working both in the academic world and commercial setting. CORE has developed a fruitful partnership with FormsVision, which the Unit first engaged with under a FP7 EU funding framework, and has successfully deployed the ALEA eCRF (electronic Case Report Form) to support trials within the UK and New Zealand. The CORE team offer a range of services which include: Database build. (CRFs, randomisations, drug supply management and ePRO (ALEA)). Data hosting (ALEA hosting for data/videos/images/documents). Expert advice (including funding application, statistics support and writing a protocol advice). -
19
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. -
20
Zelta
Merative
Zelta is a cloud-based unified clinical data management and acquisition platform with adaptable modules that can be tailored to meet the unique needs of your clinical trials program and accelerate outcomes. It offers features such as electronic data capture, clinical operations tools like randomization and trial supply management, clinical trial management system, electronic trial master file, and patient and provider engagement solutions including electronic clinical outcome assessments and electronic consent. Zelta is designed to manage clinical studies across all phases, therapeutic areas, and regions, providing a user-friendly interface and seamless access through single sign-on from anywhere in the world. The platform emphasizes flexibility and scalability, allowing for customization to align with specific study goals and the integration of solutions from both Zelta and other technology vendors. -
21
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. -
22
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. -
23
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 -
24
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. -
25
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. -
26
cubeCDMS
CRScube
cubeCDMS is an electronic data capture solution designed for clinical trial operations that streamlines the end-to-end data collection and management workflow. The system supports full data-management workflows including automatic protocol-violation detection, batch query management and native risk-based monitoring to help improve data quality and operational efficiency. The intuitive, no-code user interface enables study teams to build eCRFs (electronic case report forms) from a library of more than 55 ready-to-use forms and edit checks, quickly set up the database, and reduce start-up time. Designed for usability, cubeCDMS allows data entry once and flows data seamlessly across other integrated CRScube modules, reducing redundancy and reconciliation. Additional benefits include AI-powered medical-coding support, drag-and-drop form builders, multi-language support, and robust audit trails and change-history tracking. -
27
secuTrial
interActive Systems
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. secuTrial® is a powerful, web-based software solution for clinical trials. It enables patient data for clinical multi-center studies to be collected and managed entirely via the Internet. Full compliance is ensured with all licensing and data privacy regulations while guaranteeing the highest quality standards. -
28
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. -
29
Data+ Research
Next-Step
Jump-start your project by choosing one of our applications as your foundation to configure and modify. Can’t find what you’re looking for? Create a new app from scratch using our intuitive visual designer. With powerful pre-built components at your disposal, you can define your forms, build your workflows, and design your app with a user-friendly drag-&-drop interface. No coding required! Build your study using an intuitive visual designer and drag-&-drop interface. Define the structure of your database according to the type of study and data you need to collect. Aggregate and review your data through specialized screens. Check for discrepancies, manage incomplete forms, track follow-ups and more. Rediscover your database and organize it into manageable units according to the criteria you choose. Create filters in natural language and use saved datasets for reporting, workflow planning, patient management, data analysis and more.Starting Price: $588 per user per year -
30
Ripple Science
Ripple Science
Ripple is a web-based software solution and active registry that facilitates the recruitment and management of research participants for clinical, translational and social science studies. Built from the ground up by researchers for researchers to truly transform participant workflow, Ripple is an end-to-end research participant management software that accelerates the entire research life cycle. Applying technology to solve patient recruitment and retention challenges, the #1 reason cited when clinical trials fail. The success of clinical trials and translational studies greatly depends on the ability of research teams to meet enrollment targets on time and on budget. Ripple Recruit empowers research teams with the automation tools and analytics necessary to accelerate the recruitment processes and maximize the likelihood of study success. Ripple Recruit provides critical insights into your recruitment campaign and workflows, including what sources are most effective. -
31
YPrime
YPrime
eCOA and digital technologies are the future of clinical research, effectively bridging the gap between traditional and forward-looking, patient-focused development. Rely on YPrime’s eCOA solutions not only for high quality patient data, but for a different and better user experience -- across sponsors, investigator sites and patient users. YPrime employs an agile software development approach to quickly customize and configure functions tailored to the needs of the study in 8-12 weeks. Our interactive and visual build process ensures clients have opportunities to see the system at different stages during design and development, prior to go-live. Our pre-validated, configurable authoring environment facilitates start-up timelines and post-production changes, such as protocol amendments. -
32
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. -
33
iMotions
iMotions
The world’s leading human behavior research tool. The iMotions software is your research solution for any kind of lab research. Whether you are working within behavioral science, doing observations, studying human factors, conducting usability testing or working in a simulation environment, iMotions is your answer. Complete stimuli presentation (images, videos, websites, games, mobile/apps and VR). Integrates and synchronizes all types of sensors (eye tracking, Facial Expression Analysis, electrodermal activity aka GSR, EEG, ECG, EMG). Includes API to import/export transfer data from other sources. Built-in survey tool to add questionnaires to the data set. Live and post markers for annotations and behavioral coding. Complete study editing and analysis using embedded R-scripting to visualize data. Scene and respondent recordings and replay. Build study design by point and click.Starting Price: $2,900 per year -
34
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 -
35
CSAM Studies
CSAM Health
CSAM Studies (previously MedSciNet Studies) is a secure, highly customizable online environment with a 20-year track record of successfully hosting clinical studies and trials of all scopes and sizes. A web-based platform for medical research, Studies offers a sophisticated online application package for hosting, maintaining, and monitoring projects of every size and complexity. CSAM MedSciNet’s standard Studies solution features the complete set of components required for setting up a fully functional study or clinical trial. The benchmark solution provides support for rich and interactive data entry forms and flexible workflow structures, as well as advanced data validation, analysis, and exporting capabilities. -
36
EDC Made Easy
AB Cube Germany GmbH
AB-Cube Germany GmbH, (formerly XClinical), is a leading European provider of eClinical technologies and the developer of the Marvin EDC platform. Marvin offers an integrated suite of clinical modules, including EDC, IWRS/RTSM, Medical Coding, ePRO, and advanced reporting tools, designed to support complex and oncology-focused clinical trials. With more than two decades of experience and a strong commitment to data quality, compliance, and innovation, AB-Cube Germany empowers sponsors, CROs, academic and research institutions worldwide to conduct efficient, high-integrity clinical studies. -
37
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 -
38
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. -
39
Flatiron Horizon
Flatiron
Flatiron Health's Evidence Solutions offer a flexible approach to generating both prospective and retrospective real-world evidence, empowering life sciences companies to achieve their oncology research goals more efficiently. Central to these solutions is Flatiron Horizon, which integrates a vast repository of over 5 million de-identified patient records and 1.5 billion data points, advanced curation methods, and disease-specific machine-learning models. This platform supports various stages of the biopharma lifecycle, including discovery, clinical study design, regulatory submissions, and post-marketing commitments. Flatiron's services encompass real-world data configurations tailored to specific oncology needs, prospective evidence generation through low-interventional studies, protocol optimization, patient identification, and seamless EHR-to-EDC data transfer via Flatiron Clinical Pipe. -
40
Kymolog
Saga IT
Kymolog is a medical-device data integration and research platform for hospitals, medical-device makers, and research teams. Its edge agent captures readings from continuous glucose monitors, ECG monitors, pulse oximeters, blood-pressure cuffs, and thermometers, then represents measurements as FHIR R4 Observations with LOINC codes, UCUM units, device identity, and measurement time. Kymolog matches readings to patients and encounters using bed or device assignments and delivers them to a hospital’s existing EHR through FHIR R4 or an HL7 v2 interface engine. The same readings can be retained in a research store with their device and time provenance for clinical research and post-market evidence workflows. The software can run on premises, in a hospital-controlled private cloud, or in a device maker’s cloud; an optional hosted research store receives de-identified readings. Device classes beyond the supplied mappings can be configured. -
41
Scholarcy
Scholarcy
Scholarcy, the online article summarizer tool, reads your research articles, reports, and book chapters in seconds and breaks them down into bite-sized sections – so you can quickly assess how important any document is to your work. By identifying key information such as study participants, data analyses, main findings, and limitations, researchers and students tell us the time spent appraising a study is reduced by over 70%. As an article summarizer tool, Scholarcy creates a summary flashcard of any article, report, or document in Word or PDF format. It creates links to open-access versions of cited sources and can be configured to extract figures, tables, and images. Scholarcy helps you to speed-read the article, follow the arguments, and take away the main points in minutes. And if you’re looking for the referenced article – they’re only a click away.Starting Price: $7.99 per user per month -
42
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 -
43
Time Study RN
Rapid Modeling Corporation
Time Study RN was developed in 2002 for a Robert Wood Johnson initiative called “Transforming Care at the Bedside” or TCAB. The initiative was formed because of an observed trend that technology, new unit design, and new Nursing processes were causing the Nurse to spend less time at the bedside. At the same time, lean and Six Sigma success stories in manufacturing were catching the attention of healthcare organizations globally. Using work activities from a time study research project completed at Clarion health and published by the Institute of Medicine, RMC and the pilot TCAB teams developed the 71 work activities and 7 categories for the TCAB measurement, and RMC developed and integrated the study software and tools that formed the TCAB methodology for measuring time at the bedside. -
44
Omda MedSciNet
Omda
Omda MedSciNet solutions improve the quality, utility, and management of medical data from collection to analysis. This secure standardized software makes it easy for clinical researchers and other professionals in medicine and academia to gather and analyze well-managed medical data. The Omda team specializes in building and managing tailor-made database applications and designing clinical studies for medical research and quality registers. The Omda MedSciNet study platform provides a reliable, feature-rich, and highly customizable online environment for hosting and managing sophisticated study and clinical trial systems. Omda MedSciNet has a 20-year track record of successfully hosting studies and clinical trials of all scopes and sizes. The standard implementation includes a comprehensive set of components necessary for establishing fully functional studies or clinical trials. -
45
Buzz 3D
Buzz 3D
Retail Innovation Testing - helping retailers, FMCG brands and shopper research teams bridge the 3-silo problem of handover friction between planograms, surveys and behavioural data by making it possible to create, test and refine many more merchandising concepts than ever before. From raw shelf data to interactive survey links in minutes, Buzz is the ideal pre-screening solution before committing to deeper research. Pharmaceutical Human Factors Studies - transforming production-ready packaging artwork into interactive virtual packs that accelerate formative Human Factors evaluation, Label Comprehension and Packaging Evaluation studies before physical prototyping. Resulting study data accepted by the FDA as part of regulatory submissions. Teams are always under pressure to make better decisions, faster. Buzz 3D brings speed, scale and savings to these traditionally slow and expensive processes.Starting Price: Retail : £487 -
46
Arone
Arone
With over 20 years of experience in both software edition and clinical research sectors, Arone provides clinical research organizations with a complete suite of tools for patient data entry and management. Our solutions are turnkey and our team provides you with personalized support for the proper conduct of your projects and studies. Collect and manage patient data in a single tool. Arone manages the randomization of patients by randomly assigning study participants a type of treatment in order to remove bias in the study. Empower participants of clinical trials for their daily data entry. Benefit from a customized support for your projects. -
47
uMotif
uMotif
uMotif is a modern eCOA/ePRO and eConsent platform designed to power clinical and real-world research. Developed in collaboration with patients, the platform delivers unrivaled engagement, transforming the speed, quality, and accuracy of data. By combining uMotif's eCOA/ePRO with continuous glucose monitoring data capture, the platform delivered unprecedented data compliance rates for a pan-European diabetes study. In an immunology study, the patient-centered eCOA/ePRO solution helped the sponsor complete data capture requirements six months early. In an FDA-required CNS study, participants were engaged to capture submission-ready ePRO through their own devices. uMotif has always designed for patients first, with a relentless focus on understanding the patient journey and what drives patient behavior. This deep knowledge allows the design of software that best meets the needs of patients and delivers exceptionally high levels of engagement to study sponsors. -
48
studioMED+
studio.201 software
In no other country in Europe is more research done than in Germany. Over 600 clinical and non-clinical studies are conducted annually. As is true of any study, it is becoming increasingly complex to conduct and manage. You know that: Appointments and employees have to be coordinated, study data have to be brought up to date and documents always have to be at hand for queries. Declare war on the paper economy and exchange heavy files for a handy tablet, find information in seconds with just one click and use your valuable time for what really counts: your research. The digital study management from studioMED+ will help you with this. No matter when, no matter where: With studioMED+ you get a flexible tool that adapts optimally to your requirements.Starting Price: $200 per month -
49
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. -
50
Rally
Rally
UX researchers and designers spend hours each week manually sending emails, coordinating calendars, buying gift cards, and updating messy spreadsheets, all just to talk to users. Rally streamlines your research process by automating outreach, scheduling, and incentives. Cut out the tedious manual work of recruiting so you can focus on what matters most: doing meaningful research. Rally brings all of your participants and studies together, lets you know when participants are eligible for new studies, and makes it easy for you to launch your next study with confidence. Set up templates for every type of outreach, then schedule and sequence emails. Screeners with skip logic and auto-qualification to quickly find your best-fit participants. Team scheduling that dynamically updates your availability, and supports moderators and observers. Send incentives that are easy for you to manage and your participants to claim.
