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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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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
Visual Planning is a full-scale Clinical Trial Management System designed for those in the biotech industry. Sign up for a free demo!
Learn more about Visual Planning
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
RealTime eClinical Solutions simplifies the operations and management of clinical trials with a customizable eClinical system.
Learn more about RealTime-CTMS
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
eTMF Master allows easy upload and management of content, flexible search capabilities, and dashboards providing actionable insights.
Learn more about eTMF Master
Create and manage your Trial Master File (TMF) easily
with eTMF Master. Anju’s regulatory compliant system
lets you upload, index, review, and approve your
trial documents seamlessly in an easily configurable,
structured content repository. Built on Anju’s enterprise content management solution, eTMF Master stores all trial documents required to maintain an inspection-ready trial master file and includes flexible, role-based access control and dashboards providing actionable insights.
Learn more about eTMF Master
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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
Anju Software's CTMS Master is a clinical trial management tool that helps conduct clinical research and create reports.
Learn more about CTMS Master
Anju Software's CTMS Master is a clinical trial management tool that enhances control and visibility in clinical trial management, streamlines manual operations and addresses technical challenges.
Learn more about CTMS Master
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 simple and intuitive EDC both powerful and flexible in its configuration. Build your study up in just hours with no coding at all.
Learn more about ShareCRF
ShareCRF is a modern clinical data capture system (EDC), that allows you to build your study in just hours without having to program a single line of code. You can make mid-study changes in minutes in a completely safe way thanks to its Test Environment. Keep data from different sources (eCRF, ePRO, randomization, files, medical coding, imports, DICOM,etc.) in the same place with no effort. Besides, you won’t have to worry about servers, installations, updates or software validations.
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
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 is a leading provider of decentralized and hybrid clinical trial solutions to democratize research. With the highest-rated eClinical platform for decentralized and hybrid clinical trials, Castor’s plug-and-play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment, consent, and real-world data capture.
Castor is bringing human-centered design to the clinical trial process, from recruitment to analysis, and improving the quality, security, and reusability of data for researchers worldwide.
Users can build studies on Castor within hours leveraging pre-built templates. 90% of studies in Castor are built and pass UAT in less than 4 weeks, significantly faster than the industry benchmark. Castor also enables users to integrate EMR/EHR, patient, clinical and device data in one platform.
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
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
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
Cloud-based service that allows you to create anything from simple websites to complex applications for businesses of all sizes.
Google Cloud Platform is cloud-based service that allows you to create anything from simple websites to complex applications for businesses of all sizes in all industries. Google Cloud Platform offers a scalable data warehouse powered by cloud storage and machine learning, as well as relational databases for transactions, complex queries, and more.
New customers get $300 in free credits during the first 90 days after exhausting free usage which is available across 20+ different products.
Learn more about Google Cloud
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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
ResearchManager integrates Data Management (EDC, ePRO, RTSM, eConsent) and Clinical Operations (CTMS, eTMF, LIMS, RIMS) effectively.
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. Our EU-based data centers meet TIER 3+ standards, with Microsoft Azure Cloud services available for data localization.
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
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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
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
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
Clinical Conductor is the leading CTMS for research sites, site networks, hospitals, and health systems.
Advarra Clinical Conductor is the leading CTMS for collaborating across multiple trials and sites. Generating savings with robust finance tools, it also streamlines remote study management. With 40,000+ studies, including 20% of COVID-19 clinical trials, all receive dedicated support. Clinical Conductor is part of a suite offering eReg document management, remote monitoring ready eSource, mobile friendly eConsent, secure Video, instant payment debit cards and 2-way texting from one supplier.
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
TrialKit powers your clinical trials with technology that allows ALL users to collect, access, and manage study data from anywhere.
TrialKit, a cloud-based platform available via a web interface and downloadable native mobile app, enables end-to-end clinical trial management for pharmaceutical, biotechnology, and medical device companies of all sizes. Design and deploy regulatory compliant studies in days instead of weeks using our intuitive forms designer that requires no programming.
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
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
