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Clinical Trial Management Software
Clinical Trial Management software helps manage all aspects of clinical trials including patient data, scheduling, reporting, analysis, and data management.
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ResearchManager combines Data Management (EDC, ePRO, RTSM, eConsent) with Clinical Operations (CTMS, eTMF, LIMS, RIMS) in one platform.
Learn more about Researchmanager – Clinical Research Suite
ResearchManager Clinical Research Suite is a centralized platform for clinical research, providing comprehensive access and control over every stage of a trial.
As a Software-as-a-Service (SaaS) solution, the Clinical Research Suite adapts seamlessly to the specific needs of clinical trials, offering a range of products for Clinical Operations (CTMS, eTMF, LIMS, RIMS) and Data Management (EDC, ePRO, RTSM, eConsent).
ResearchManager is compliant with ISO, GCP, GDPR, and HIPAA standards, operating from headquarters in the Netherlands and the USA.
Customers can choose between TIER3+ EU-based data centers and cloud solutions that offer regional data storage in locations like the USA, Canada, and Australia.
Choose the flexibility of the On Demand plan or scale with the Enterprise plan. Get a cost estimate within 1 minute on our website, and/or schedule a demo with one of our specialists.
Learn more about Researchmanager – Clinical Research Suite
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Electronic trial master file (eTMF) solution with intuitive workflows for managing clinical studies.
Learn more about Florence eTMF
Florence Electronic trial master file (eTMF) is the only eTMF that combines ease of use with integrated remote access to study sites on the Florence platform.
Implementing an eTMF is critical for Sponsors
and CROs that want to increase
study capacity, and enable more trials.
With over 10,000 research sites connected to
the Florence Network, we have an intimate
understanding of the research site and the site’s
eISF where over 80% of a TMF’s documents
originate.
Learn more about Florence eTMF
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Create a digital connection to every site in your study on a platform they already love and use in their workflows.
Learn more about Florence SiteLink
SiteLink™ facilitates 5.2 million remote workflows
every month across 18,000 study sites in 52 countries.
Activate remote site start-up, monitoring, and source data review/verification on SiteLink™. Connect and deploy Florence eBinders™, the industry-standard electronic Investigator Site File (eISF) and Electronic Participant Binder, on a global scale to every site in your study.
Florence eBinders is ranked #1 for clinical trial workflows by sites for ease of use, ease-of-setup, and support.
Learn more about Florence SiteLink
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Helps streamline document workflows, compliance, and more for clinical trials.
Learn more about Florence eBinders
Digitize all of your study binder workflows with Florence eBinders™ and provide remote access for start-up, monitoring, and source data review for your sponsors. eBinders is trusted by 18,000+ research sites around the globe.
Create, edit, distribute, collect, sign and review all investigator site files, electronic logs and participant binders electronically within a single platform. Speed study start-up by as much as 40%.
Learn more about Florence eBinders
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
User-friendly, flexible, web-based electronic data capture (EDC) and data management system for clinical trials and research.
Learn more about Dacima Clinical Suite
User-friendly, flexible, web-based electronic data capture (EDC) and data management system for clinical trials, epidemiological research, web randomization (IWRS), patient registries, ePRO and web surveys. Our software provides the most easy to use and intuitive interface on the market with features and design options not available in other software products.
Learn more about Dacima Clinical Suite
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Are your study data working for you, or are you working for them? Control, compliance, and adaptability shouldn’t be a struggle.
Learn more about ShareCRF
Managing clinical trial data doesn’t have to be complicated. What if you could set up your study in hours, without coding or waiting for external help? With an intuitive interface, ShareCRF puts you in control, letting you configure everything yourself.
Compliance? We've got you covered. ShareCRF is a validated platform designed to meet regulatory standards, so your data stays safe, reliable, and audit-ready.
And adaptability? Your study is unique, and your tools should reflect that. Whether it’s a simple setup or a complex trial, ShareCRF adjusts to your needs without forcing you to compromise.
Because efficient, compliant, and flexible data management isn’t just a luxury—it’s what every study deserves.
Learn more about ShareCRF
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Validated CTMS with inbuilt eTMF. Cloud-based & on-premise options. Scalable system for CROs, pharma, biotech, and medical devices.
Learn more about Flex Databases platform
Flex Databases is a secure, unified and compliant system specifically built for life sciences.
All modules are validated and compliant with 21 CFR Part 11 and GxP requirements, and other global regulations.
Our system consists of modules that cover clinical, quality and compliance, safety, as well as project and finance management, from project start-up to product production and post marketing
Flex Databases CTMS offers a modular design, allowing you to tailor it to your specific trial needs. You can choose only the modules you require and have the flexibility to add or remove them as your trial progresses.
For deployment options, Flex Databases CTMS caters to both cloud-based and on-premise preferences.
Learn more about Flex Databases platform
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Capture and integrate data from any source into one easy-to-use platform: EDC, eConsent, ePRO, eCOA, Digital Enrollment, DCT & eSource.
Learn more about Castor EDC
Castor EDC is a comprehensive clinical research platform that enhances how clinical trials are run. It offers EDC, ePRO, and eConsent solutions, all aimed at improving data collection and clinical operations to accelerate the delivery of therapies, drugs, and devices to market safely. Castor prioritizes patient and site experience, integrating the human element into all aspects of its tech.
With experience in 15,000 studies with 8 million patients across 90 countries, Castor is adept at managing complex trials. Its cloud-native platform supports flexible deployment of modules for recruitment, data capture, & more, tailored to study requirements. Utilizing Practical AI and an API-first strategy, Castor simplifies the research process. Researchers can collect and analyze data from sources including clinics, homes, and wearables. Castor's flexible, robust technology advances clinical research accessibility and efficiency, promotes evidence-based medicine, and enhances global health.
Learn more about Castor EDC
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Smartsheet is an online work execution platform empowering organizations of all sizes to plan, manage, automate, and report on work.
Smartsheet, an online work execution platform, empowers pharmaceutical companies and clinical research organizations to track, manage, and report on clinical tests and trials. With its familiar spreadsheet format, Smartsheet enables teams to easily get started and effectively collaborate. Securely share, store, and access PHI while meeting HIPAA's regulatory requirements. Plus, real-time dashboards allow you to spend less time on the process and more time delivering results.
Learn more about Smartsheet
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Sales Execution Platform built to help you sell faster. Prioritize leads & tasks, recommend actions, and help your team execute them.
LeadSquared’s Healthcare CRM is a comprehensive solution that complies with 21 CFR Part 11 and HIPAA, ensuring secure data capture, transfer, and management. It offers seamless EMR/EHR integration, efficient patient management, and robust scheduling capabilities. It also provides document management, Clinical trial Management and inventory management features. LeadSquared enhances workflow management, supports patient recruiting. All these features contribute to improved productivity.
Learn more about LeadSquared
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Viedoc is a trusted eClinical solution for designing, managing, and executing clinical studies. Used in 75+ countries, powering 1000s.
Viedoc is an eClinical solution that allows you to design, manage and execute clinical studies in one scalable system. Since 2003, Viedoc has been used to power thousands of studies by collecting data from over a million patients in over 75 countries.
The Viedoc solutions support major pharmaceutical, biotech, and medical device companies and renowned research institutions worldwide by accelerating clinical trials on all levels.
Learn more about Viedoc
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
RealTime eClinical Solutions simplifies the operations and management of clinical trials with a customizable eClinical system.
RealTime eClinical Solutions is a leading technology provider reshaping the operations and management of clinical trials with its comprehensive eClinical system. Purpose-built for clinical research sites, site networks, AMCs, sponsors, and CROs, the platform goes beyond traditional CTMS to empower research and business workflows for modern-day clinical trials from trial award and study start-up through to trial execution. RealTime helps organizations manage the research and business of clinical trials, together, with electronic solutions including CTMS, eReg/eISF, eSource, participant payments (SitePay/GlobalPay), engagement solutions (Text, eConsent, and MyStudyManager™ Participant Portal), and Devana for pipeline management, business intelligence, and process and performance metrics.
Learn more about RealTime-CTMS
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Medrio provides fast and easy-to-use eClinical solutions with no programming required in a traditional, hybrid or virtual setting.
Medrio empowers faster, higher-quality clinical trials with greater control. With almost two decades of experience, Medrio delivers proven, scalable solutions, unrivaled customer support, and guidance to industry innovators. Our suite of solutions, including CDMS/EDC, eCOA/ePRO, eConsent and RTSM, enables the capture of quality clinical trial data while optimizing workflows for regulatory readiness. Experience the power of Medrio and realize the full potential of your clinical operations.
Learn more about Medrio
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Visual Planning is a full-scale Clinical Trial Management System designed for those in the biotech industry. Sign up for a free demo!
Visual Planning is a full-scale scheduling and CTMS platform designed for those in the Clinical Trial industry. Configured with researchers in mind, oversee project milestones, research budgets, data management & more with Visual Planning’s popular scheduling tools. Manage real-time reports, projects, and assets across all devices for a singular management platform. Tailor a Clinical trial software solution that meets your institution’s needs. Sign up for a free demo today!
Learn more about Visual Planning
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Study design, EDC, ePRO, IxRS and rich data visualizations - all on one user-friendly platform. This is your clinical data, managed.
Offering leading biotech and pharmaceutical companies, CROs, academic institutions, and government agencies the foundational clinical data management tools they need (EDC, ePRO/eCOA, RTSM, and reporting) with innovative, next-generation technology (EHR/eSource, RWD, and DCTs) to drive the future of digital clinical trials.
Learn more about OpenClinica
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
CTMS/ eSource/ eDocs/ Text SMS/ Recruitment Automation/ Integrated Calendar and many more powerful tools for Clinical Research Sites
eClinPro is the most affordable integrated multi-functional system for all sizes of Clinical Research Sites. CTMS/ eSource/ eDocs/ Text SMS/ Recruitment Automation/ Website Integration/ Integrated Calendar and many more powerful tools providing the perfect solution for Clinical Research Sites. The system was designed by CRCs, CRAs, Managers, PIs, facilitating the entire process since the recruitment starts to the closeout.
Learn more about eClinPro CTMS & eSource
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
End-to-end clinical trials made easy—design, collect, and manage data anywhere with TrialKit’s web and mobile app access.
TrialKit is a powerful cloud-based platform designed for end-to-end clinical trial management, accessible anytime, anywhere via a web interface or native mobile app. Built for sponsors and CROs of all sizes, TrialKit empowers users to streamline study design, data collection, and management in a single platform. Its drag-and-drop form builder allows you to create and deploy regulatory-compliant studies in days, not weeks. Recognized with the 2024 SCDM Innovation Award for Health Technology Solutions, TrialKit's latest AI-driven technology, TrialKit AI, takes clinical data analysis and reporting to the next level. From site to sponsor, every stakeholder can securely collect, review, and analyze data in real-time. Whether on the go or at your desk, TrialKit ensures seamless workflows and unmatched flexibility, helping you save time and reduce costs while maintaining compliance. Simplify your complex clinical trials with a solution that puts efficiency and accessibility at the forefront.
Learn more about TrialKit
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Clinical Conductor CTMS provides comprehensive research operations management for sites, site networks, hospitals, and health systems.
Clinical Conductor is a clinical trial management system (CTMS) built to streamline research operations for research site networks, health systems, and independent research sites. Clinical Conductor provides in-depth management across a site's research portfolio, including financial management, patient recruitment, protocol and participant management, and much more. It is also seamlessly connected to Advarra's suite of technology solutions, including Advarra eReg and Advarra eSource. These systems are used by hundreds of research sites to optimize workflows and help manage their research as a business.
Learn more about Clinical Conductor CTMS
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Ripple facilitates the recruitment & management of patients for clinical and translational studies from pre-enrollment to study end.
Ripple is a highly-secure, web-based, retention-focused patient and study management tool for clinical and translational study teams. Ripple streamlines your study processes and centralizes all aspects of recruitment and post-enrollment tracking of patients in clinical trials. Ripple helps clinical trial sites enroll more patients faster, manage engagements, simplify reporting, and automate tasks in order to provide an efficient, patient-centered experience to all trial participants.
Learn more about Ripple
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
A global, innovative, cloud-based clinical research management system providing faster access to real-time data.
EDGE is a global clinical research management system which is embedded into the clinical research infrastructure across 80% of England’s NHS regions, as well as prominently across Scotland and Northern Ireland. Overseas, EDGE is utilised in Canada, New Zealand, Belgium, South Africa, and India. EDGE offers a unique approach to the management and conduct of research through purpose-built software and provides research professionals with fast access to real-time data.
Learn more about EDGE
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Create powerful mobile forms, collect data offline and visualize it with a few clicks.
Teamscope is the worlds easiest to use data collection app for clinical and field research.
With Teamscope you can build powerful forms with branching logic, data validation and automatic calculations. Use mobile forms to collect data without the need for an internet connection. Create cases, share them with your team and capture data across time. Keep your data secure at all moments with a passcode and data encryption.
Learn more about Teamscope
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences.
Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences.
Veeva Vault is the only content management platform with the unique capability to manage both content and data. Because all Vault applications are built on the same core platform, companies can ease the flow of documents across regions and departments, eliminating system, site, and country silos and streamlining their end-to-end clinical processes.
Learn more about Veeva Vault
...
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
CRIO, the leader in eSource technology, is built for site workflows. CRIO exists at the intersection between sites, sponsors and CROs.
An intuitive eSource, lab routing, and CTMS solution for research sites. Using CRIO, sites can save favorite procedures; build customized source templates; capture source data quickly and accurately; mark up labs; and share visits with their monitors for review. Recruiting helps manage patients and campaigns, and enables one-click calling and texting. Finances calculates receivables and invoiceables as the visits are being completed. We are a premium service at an affordable price.
Learn more about CRIO
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Xolomon is an online solution for the creation of databases and web apps, specialized in collecting and exploiting clinical information
Xolomon is an online solution for the creation of databases and web applications, specialized in collecting and exploiting clinical information.
Xolomon allows for a quick, simple and customized creation of applications such as: electronic case report forms (eCRF) for clinical studies, ePROs, patient registries, electronic medical records, Clinical Trial Managers (CTMS),...
We combine agility, speed of development and ease of use with the highest industry standards for data protection.
Learn more about Xolomon
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
Manage, distribute and optimize your content across premium publishers through 25+ social, native and content discovery partners.
Story by PulsePoint makes content marketing more efficient, more effective and more trackable.
We extend your targeted reach across premium social, native, and content discovery channels. Our
platform optimizes to your KPIs to maximize engagement and deliver clear ROI.
How it works: Upload your content via URL and create multiple headline/image variants for each channel seamlessly, choose your channels you want to advertise on. Story optimizes towards KPIs.
Learn more about Story
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Features
- Financial Management
- Data Capture and Transfer
- Scheduling
- Data Import/Export
- Electronic Data Capture
- Workflow Management
- Patient Monitoring
- Patient Management
- 21 CFR Part 11 Compliance
- Document Management
- Inventory Management
- Patient Recruiting
