---
description: Discover the best Clinical Trial Management Software for your organisation. Compare top Clinical Trial Management Software tools with customer reviews, pricing and free demos.
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title: Best Clinical Trial Management Software - 2026 Reviews, Pricing & Demos
---

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# Clinical Trial Management Software

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## Products

1. [RealTime-CTMS](https://www.softwareadvice.com.au/software/105354/realtime-ctms) — 4.9/5 (65 reviews) — RealTime-CTMS is a web-based clinical trial management system. It is designed for sponsors, CROs, research sites, uni...
2. [ShareCRF](https://www.softwareadvice.com.au/software/357170/sharecrf) — 4.8/5 (44 reviews) — Managing clinical trial data shouldn’t be a constant challenge. ShareCRF is designed to make your life easier, empowe...
3. [Castor EDC](https://www.softwareadvice.com.au/software/109506/castor-edc) — 4.7/5 (204 reviews) — Castor is an advanced Electronic Data Capture (EDC) platform designed to streamline clinical research by enabling fas...
4. [Castor ePro](https://www.softwareadvice.com.au/software/420255/castor-epro) (0 reviews) — Castor ePRO: Full-Service eCOA for Modern Clinical Trials Castor ePRO is a fully validated, cloud-based solution for ...
5. [EDGE](https://www.softwareadvice.com.au/software/220291/edge) — 4.9/5 (35 reviews) — EDGE is a clinical trial management solution that provides reporting capabilities to speed up internal processes and ...
6. [Smartsheet](https://www.softwareadvice.com.au/software/157390/smartsheet) — 4.5/5 (3482 reviews) — Smartsheet is a work execution platform and collaboration tool with a familiar spreadsheet-like interface that helps ...
7. [Researchmanager – Clinical Research Suite](https://www.softwareadvice.com.au/software/108609/research-manager) — 4.2/5 (112 reviews) — ResearchManager offers a sophisticated, flexible, and cost-effective eClinical platform encompassing Clinical Data Ma...
8. [Viedoc](https://www.softwareadvice.com.au/software/365099/viedoc) — 4.4/5 (95 reviews) — At Viedoc, we design intuitive eClinical solutions that streamline every phase of clinical research. With over 20 yea...
9. [Visual Planning](https://www.softwareadvice.com.au/software/3673/visual-planning) — 4.5/5 (90 reviews) — Visual Planning is a powerful, customizable platform designed to help businesses plan, schedule, and manage resources...
10. [Florence eBinders](https://www.softwareadvice.com.au/software/371223/ebinders) — 4.5/5 (83 reviews) — Florence eBinders is an electronic solution that digitizes, automates, and integrates the investigator site files, pa...
11. [Medrio](https://www.softwareadvice.com.au/software/105219/medrio) — 4.6/5 (51 reviews) — Medrio empowers faster, higher-quality clinical trials with greater control. With two decades of experience, Medrio d...
12. [OpenClinica](https://www.softwareadvice.com.au/software/104919/openclinica) — 4.6/5 (37 reviews) — OpenClinica is a clinical data management and electronic data capture solution designed to help medical institutions ...
13. [eClinPro CTMS & eSource](https://www.softwareadvice.com.au/software/239553/eclinpro) — 4.6/5 (36 reviews) — eClinpro is a cloud-based clinical research software suite. It caters to pharmaceutical companies, CROs, and research...
14. [TrialKit](https://www.softwareadvice.com.au/software/239899/trialkit) — 4.5/5 (34 reviews) — TrialKit, developed by Crucial Data Solutions, is a unified eClinical platform designed to simplify how clinical tria...
15. [Clinical Conductor CTMS](https://www.softwareadvice.com.au/software/105345/clinical-conductor-ctms) — 4.5/5 (33 reviews) — Clinical Conductor CTMS (CC CTMS) is the leading clinical research management solution, utilized by more sites in the...
16. [Ripple](https://www.softwareadvice.com.au/software/105261/ripple) — 4.8/5 (32 reviews) — Ripple is a web-based solution designed to manage recruitment and post-enrollment tracking of clinical trial patients...
17. [Veeva Vault](https://www.softwareadvice.com.au/software/13108/veeva-vault) — 4.4/5 (28 reviews) — Veeva Vault is a cloud-based content management solution with built-in collaboration features designed specifically f...
18. [Health Cloud](https://www.softwareadvice.com.au/software/319387/salesforce-health-cloud) — 4.4/5 (23 reviews) — Salesforce Health Cloud is a patient management platform designed to help medium to large healthcare organizations ma...
19. [ClinCapture](https://www.softwareadvice.com.au/software/105231/clincapture) — 4.9/5 (21 reviews) — Captivate EDC is a cloud-based electronic data capture solution that assists medical researchers and practitioners wi...
20. [CRIO](https://www.softwareadvice.com.au/software/307073/clinical-research-io) — 4.5/5 (21 reviews) — CRIO is a health tech company delivering comprehensive clinical research solutions for pharma, biotech, research site...
21. [Xolomon](https://www.softwareadvice.com.au/software/204376/xolomon) — 4.0/5 (20 reviews) — Xolomon is an electronic medical record (EMR) and patient engagement solution that helps healthcare organizations str...
22. [Florence eTMF](https://www.softwareadvice.com.au/software/385936/florence-etmf) — 4.6/5 (18 reviews) — Get set up fast with the top-rated platform in ease-of-use, ease-of-setup, and customer support. Plus, connect direct...
23. [RegDocs365](https://www.softwareadvice.com.au/software/249010/regdocs365) — 3.8/5 (18 reviews) — RegDocs365 is an electronic regulatory document management (EDM) system for life sciences. It caters to biotech, phar...
24. [STARLIMS](https://www.softwareadvice.com.au/software/359070/starlims) — 4.2/5 (17 reviews) — STARLIMS is a clinical trial management software that helps businesses collect, manage and interpret laboratory data....
25. [Medidata CTMS](https://www.softwareadvice.com.au/software/458480/Medidata-CTMS) — 4.3/5 (17 reviews) — The Clinical Trial Management System (CTMS) offered by Medidata Solutions is a platform designed to enhance the effic...

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- [Electronic Data Capture Software](https://www.softwareadvice.com.au/directory/4632/electronic-data-capture/software)

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No coding skills? No problem. Our intuitive, user-friendly interface allows you to set up forms, workflows, and settings independently, without needing outside help or technical expertise.\n\nCompliance You Can Trust\nRegulations are non-negotiable, and ShareCRF was built with this in mind. Our validated software ensures your data remains secure, traceable, and ready for any audit or regulatory review. With ShareCRF, you don’t have to worry about compliance—it’s embedded in the platform.\n\nAdaptability That Works for You\nNo two studies are the same, so why settle for a rigid system? ShareCRF adapts to your unique needs, whether it’s a straightforward study or a complex trial. Configure it to match your workflows and requirements, without compromising on quality or functionality.\n\nThe Simplicity You Deserve\nWe believe that managing your clinical data shouldn’t take away from your research. That’s why we’ve designed a platform that reduces complexity and gives you more time to focus on what really matters—delivering results.\n\nJoin the researchers, sponsors, and CROs who have already streamlined their studies with ShareCRF. Because efficient, compliant, and adaptable data management isn’t just a nice-to-have—it’s a must-have.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/890de8d8-b20c-48f4-acb7-da5d47e26011.png","url":"https://www.softwareadvice.com.au/software/357170/sharecrf","@type":"ListItem"},{"name":"Castor EDC","position":3,"description":"Castor is an advanced Electronic Data Capture (EDC) platform designed to streamline clinical research by enabling fast, seamless data collection and integration. Researchers can build and launch studies in hours using pre-built templates while effortlessly connecting EMR/EHR, ePRO, eCOA, clinical, and device data (eCRF, eSource) into a single, centralized platform. With 90% of studies passing UAT in under four weeks, Castor significantly reduces trial setup time compared to industry benchmarks.\n\nCastor’s no-code, self-service platform simplifies study management with drag-and-drop eCRF creation, automated randomization, real-time monitoring, and seamless data import/export. It also supports HL7 FHIR-based EHR integration and API connectivity, ensuring smooth interoperability with existing systems. Built for compliance, Castor meets ISO27001, ISO9001, HIPAA, GCP, 21 CFR, and GDPR standards, with robust audit trails and granular user management for complete security and oversight.\n\nDesigned for speed, scalability, and ease of use, Castor helps sponsors, CROs, and researchers accelerate trials, enhance patient engagement, and leverage real-world data (RWD) in a modern, cloud-native environment.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/f4c0fdec-0003-4776-afa2-ecedca2f2a96.png","url":"https://www.softwareadvice.com.au/software/109506/castor-edc","@type":"ListItem"},{"name":"Castor ePro","position":4,"description":"Castor ePRO: Full-Service eCOA for Modern Clinical Trials\n\nCastor ePRO is a fully validated, cloud-based solution for collecting electronic patient-reported outcomes in clinical trials. It’s built to support decentralized, hybrid, and site-based study designs—seamlessly integrated into Castor’s unified clinical trial platform alongside EDC, eConsent, and eCOA.\n\nDesigned for sponsors, CROs, and academic teams looking to simplify trial operations, Castor ePRO offers more than just software. Our dedicated eCOA services team supports you from study build through closeout. We take care of scale licensing, translation into 40+ languages, device provisioning, and direct-to-patient support in multiple regions—so your team can stay focused on science and study execution.\n\nWhether you're running a global Phase III trial or a digital study with a lean team, Castor helps you launch faster. Most full builds go live in 8–10 weeks, thanks to our modular platform and expert implementation support.\n\nKey features include:\n\nBYOD and provisioned device options\n\nOffline data collection for remote access\n\n120+ pre-validated PRO instruments\n\nConfigurable eConsent and EDC integration\n\nGlobal compliance with 21 CFR Part 11, GDPR, GCP\n\nCastor ePRO is trusted by top research institutions, biotechs, and CROs worldwide. If you're looking for a scalable ePRO solution that balances speed, service, and compliance, Castor offers the flexibility and operational support you need to run high-quality, patient-centric trials.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/e4e29a4b-6466-46fb-8432-17cdc1dc0130.png","url":"https://www.softwareadvice.com.au/software/420255/castor-epro","@type":"ListItem"},{"name":"EDGE","position":5,"description":"EDGE is a clinical trial management solution that provides reporting capabilities to speed up internal processes and enable users to maximize data utilization. This solution is used across 80% of the NHS within the UK as well as in Canada, Belgium, New Zealand, South Africa, and other countries. It is designed to help organizations improve the quality of research management.\n\nEDGE provides study and patient management workflows, a finance module, and electronic delegation logs. Studies can be tracked from beginning to end using real-time data. Other features include document storage, custom field creation, collaboration functions, shared calendars, and more. \n\nPricing is based on organization type and size. Addtional details are provided on request by EDGE.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/88f7f893-5ea8-4b8d-9dd7-afaca37d2ea9.jpeg","url":"https://www.softwareadvice.com.au/software/220291/edge","@type":"ListItem"},{"name":"Smartsheet","position":6,"description":"Smartsheet is a work execution platform and collaboration tool with a familiar spreadsheet-like interface that helps teams plan, track, and manage projects in real-time. Smartsheet features include a range of project management tools, such as document and resource management, project reporting, task management, file sharing, and timeline tracking.\n\nSmartsheet can help teams standardize a project process, maximize productivity, and improve collaboration with automated workflow options that fit individual work preferences. Within the platform's project management tools, data can be sorted using card, grid, Gantt chart, and calendar view. With a real-time dashboard, teams can track project status, manage resources, and assign tasks to improve overall visibility and work efficiency.\n\nProject plan information can be shared with leadership team members and key stakeholders to keep everyone on the same page. Activity log reports and customizable dashboards help ensure that team collaboration is consistent across projects of any size and kind, from software development to marketing plans.\n\nWith the Smartsheet app, teams can access project information and workflow data while on the go. The mobile app is compatible with iOS and Android devices.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/9efb2a2f-43b2-4ebd-bf24-b9bb46bd93c6.jpeg","url":"https://www.softwareadvice.com.au/software/157390/smartsheet","@type":"ListItem"},{"name":"Researchmanager – Clinical Research Suite","position":7,"description":"ResearchManager offers a sophisticated, flexible, and cost-effective eClinical platform encompassing Clinical Data Management Tools (EDC, ePRO, RTSM, eConsent) and Clinical Operations (CTMS, eTMF, LIMS, RIMS).\n\nBacked by a decade of experience, a user base exceeding 20,000, and a track record of over 25,000 global studies, ResearchManager is a trusted partner for CROs, Pharma, Biotech, MedTech, Academic institutions, Healthcare providers, as well as Medical Ethical Committees/IRBs","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/296f2c02-6745-463e-afe4-136a36f307e4.jpeg","url":"https://www.softwareadvice.com.au/software/108609/research-manager","@type":"ListItem"},{"name":"Viedoc","position":8,"description":"At Viedoc, we design intuitive eClinical solutions that streamline every phase of clinical research. With over 20 years of experience, our proven platform simplifies data collection, management, and analysis—empowering CROs, pharmaceutical, biotech, and academic organizations to bring life-changing treatments to market faster.\n\nTrusted worldwide, Viedoc has powered over 7,000 studies across 75+ countries, supporting more than 1.6 million participants. Our cloud-based technology ensures reliability, scalability, and ease of use, removing barriers that slow down clinical trials. Headquartered in Sweden, we also operate in the US, France, Japan, Vietnam, and China, making innovation in clinical research accessible globally.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/86e508d6-b223-4b4d-82fb-d202bc12055a.jpeg","url":"https://www.softwareadvice.com.au/software/365099/viedoc","@type":"ListItem"},{"name":"Visual Planning","position":9,"description":"Visual Planning is a powerful, customizable platform designed to help businesses plan, schedule, and manage resources efficiently across teams, projects, and industries. From construction and manufacturing to field services, clinical trials, and office-based project teams, Visual Planning adapts to your workflows rather than forcing you to adapt to the software.\n\nWith an intuitive drag-and-drop interface, you can schedule employees, subcontractors, equipment, and materials in real time. Visual Planning supports multiple views — including Gantt charts, Kanban boards, calendars, and maps — allowing managers to choose the most effective way to visualize their operations.\n\nKey Capabilities:\n\nCentralized Scheduling: Manage all tasks, events, and resources from one platform, reducing scheduling conflicts and double bookings.\n\nReal-Time Updates: Changes are instantly visible to all stakeholders, whether they are in the office or on-site, ensuring teams remain aligned.\n\nMobile & Field-Ready: The VPGo mobile app enables field workers to update job progress, submit photos, and report issues — even offline.\n\nAdvanced Resource Management: Filter resources by skills, availability, certifications, or location, ensuring the right people and tools are always assigned to the right job.\n\nBudget & Cost Tracking: Monitor labor and material expenses in real time to prevent cost overruns and keep projects profitable.\n\nIntegration-Friendly: Connect Visual Planning with ERP, CRM, HRIS, and other business tools via REST API and Webhooks, eliminating duplicate data entry.\n\nCollaboration Tools: Share schedules, assign tasks, and exchange files within the same platform to streamline communication and decision-making.\n\nIndustry-Specific Solutions: Configure templates and workflows tailored to your sector — from fleet and asset management to clinical research timelines and subcontractor coordination.\n\nWhy Businesses Choose Visual Planning:\n\nFlexibility: Fully customizable views, filters, and fields let you adapt the platform to your processes.\n\nProductivity Gains: Reduce time spent on administrative scheduling tasks by up to 30%, freeing teams to focus on high-value work.\n\nTransparency: Dashboards and reports offer instant visibility into workload, progress, and upcoming deadlines.\n\nScalability: Suitable for small teams as well as enterprise-level operations with multiple sites and hundreds of resources.\n\nWhether you need to plan complex construction schedules, manage clinical trial visits, coordinate manufacturing production, or simply keep a distributed workforce aligned, Visual Planning provides the tools to keep your operations organized, on time, and on budget.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/f57c117c-d011-4ef0-9eed-0332deee8a0b.png","url":"https://www.softwareadvice.com.au/software/3673/visual-planning","@type":"ListItem"},{"name":"Florence eBinders","position":10,"description":"Florence eBinders is an electronic solution that digitizes, automates, and integrates the investigator site files, participant binders, and logs for clinical research sites. The product serves the needs of research sites, sponsors, and contract research organizations by providing a centralized platform to manage essential regulatory and participant-related documents.\n\nThe product offers features to enhance compliance and operational efficiency. It provides role-based access, version control, audit trails, and electronic signatures to meet regulatory standards. The intuitive workflows enable rapid study setup and activation, with customizable access and permissions for the entire study team and external users. Florence eBinders seamlessly integrates with clinical trial management systems and electronic medical record/electronic health record systems, streamlining source data management and remote monitoring capabilities.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/fd62e31b-4c5a-49d7-bc9a-22208e4ce97d.jpeg","url":"https://www.softwareadvice.com.au/software/371223/ebinders","@type":"ListItem"},{"name":"Medrio","position":11,"description":"Medrio empowers faster, higher-quality clinical trials with greater control. With two decades of experience, Medrio delivers proven, scalable solutions, unrivaled customer support, and guidance to industry innovators.\n\nOur suite of solutions, including Electronic Data Capture (EDC), eCOA/ePRO, eConsent and RTSM, enables the capture of quality clinical trial data while optimizing workflows for regulatory readiness. We guide the industry's leading innovators, including within the pharmaceutical/biotech, medtech/medical device or diagnostics, animal health industries and more. Experience the power of Medrio and realize the full potential of your clinical operations.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/2bec2bf8-6b01-4721-8fb4-1d248899059d.png","url":"https://www.softwareadvice.com.au/software/105219/medrio","@type":"ListItem"},{"name":"OpenClinica","position":12,"description":"OpenClinica is a clinical data management and electronic data capture solution designed to help medical institutions capture electronic data and streamline clinical trials using electronic case report forms (eCRFs) and a drag-and-drop interface. For patient-reported outcomes, patients can respond to forms and surveys on any device of their choosing. Physicians can collect patients' information using responsive mobile forms and share operational reports with team members.\n\n\nOrganizations can create multiple treatment groups, label drug kits with randomization codes, and sort trial lists based on age, sex, test site or electronic case report forms (eCRF). Using OpenClinica, professionals can view operational data in the form of bar charts, graphs or key performance indicators and maintain organizational compliance with Good Clinical Practice (GCP), 21 CFR Part 11, and other industry standards. Additionally, clinicians can use the dashboard to import/export files, review site activities, and track the progress of ongoing trials.\n\n\nFor total study control, OpenClinica integrates and partners with Bio-Optronics to provide advanced functionality over research operations. OpenClinica also provides an open-source version, OpenClinica Community Edition, on GitHub to provide users greater control over the technology.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/91f8053c-7f03-403f-967a-22edea26ec15.png","url":"https://www.softwareadvice.com.au/software/104919/openclinica","@type":"ListItem"},{"name":"eClinPro CTMS & eSource","position":13,"description":"eClinpro is a cloud-based clinical research software suite. It caters to pharmaceutical companies, CROs, and research sites.\n\neClinpro provides a clinical trial management system (CTMS) to help manage study protocols, track milestones, and oversee study progress. The electronic source (eSource) functionality allows for collecting data electronically at the point of care using tablets and smartphones. eDocs gives users a centralized place to store and share study documentation. The text message appointment reminder feature automatically sends reminders to study participants about upcoming visits and tasks. The volunteers database management tool stores participant information and tracks enrollment status.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/0132e7b1-8add-49f2-a602-1856a1cc45c0.png","url":"https://www.softwareadvice.com.au/software/239553/eclinpro","@type":"ListItem"},{"name":"TrialKit","position":14,"description":"TrialKit, developed by Crucial Data Solutions, is a unified eClinical platform designed to simplify how clinical trials are designed, executed, and analyzed. Built for sponsors, CROs, and research sites, TrialKit brings together the core systems required to run modern studies into a single, flexible environment, eliminating the need for multiple disconnected tools.\n\nThe platform supports the full study lifecycle, from startup through closeout, with capabilities including electronic data capture (EDC), ePRO/eCOA, eConsent, randomization and trial supply management (RTSM), medical coding, imaging, eTMF, and direct data capture (eSource). TrialKit is designed to accommodate studies of any size, complexity, or therapeutic area, making it equally effective for emerging sponsors and large, multi-study portfolios.\n\nA key advantage of TrialKit is its configurability. With an intuitive drag-and-drop study builder, research teams can design and deploy regulatory-compliant studies quickly without requiring extensive programming or external support. This enables faster study startup while maintaining full control over workflows, edit checks, and data structures.\n\nTrialKit is accessible via both web and native mobile applications, allowing sites, sponsors, and participants to securely collect and review data in real time from virtually anywhere. This flexibility supports traditional, hybrid, and fully decentralized trial models while improving engagement and data quality across all stakeholders.\n\nEmbedded within the platform is TrialKit AI, recognized with the 2024 SCDM Innovation Award for Health Technology Solutions. Powered by proprietary intelligence (Floyd), TrialKit AI extends beyond traditional reporting to support advanced analytics, conversational data exploration, full study simulation, and protocol validation. These capabilities allow teams to evaluate study design decisions, identify risks earlier, and generate deeper insights from both internal and external datasets without relying on separate tools.\n\nBy centralizing data collection, management, and analysis within one platform, TrialKit reduces operational complexity, minimizes manual processes, and improves overall study efficiency. Its scalable architecture and flexible pricing model support organizations as they grow, while maintaining a strong foundation in data integrity, compliance, and performance.\n\nTrialKit is trusted by research teams globally for its balance of functionality, affordability, and support, providing a practical, modern solution for managing today’s increasingly complex clinical trials.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/40c91617-0dc2-44b5-89de-03617e0a4fa4.png","url":"https://www.softwareadvice.com.au/software/239899/trialkit","@type":"ListItem"},{"name":"Clinical Conductor CTMS","position":15,"description":"Clinical Conductor CTMS (CC CTMS) is the leading clinical research management solution, utilized by more sites in the world than any other CTMS.  Hospitals, hospital networks, health systems, large site networks, and even smaller sites are benefitting from the ability to manage finances, recruitment data, participant information, and clinical study details for virtual, hybrid and traditional trials. CC CTMS provides the most robust budgeting and billing reports, monitoring, and billing compliance tools avaialble.\n\nTo help organizations with patient recruitment efforts, CC CTMS centralizes the organization of all recruitment tasks while tracking progress from any location. Electronic signatures and online document sharing reduce the need for paperwork and streamline clinical trial processes.\n \nAdditional features include study setup, contact management, appointment scheduling, visit management, integrated eSource, eReg, eConsent options to enhance remote workflows, in addition to eVideo, ePay, and texting controlled in dashboards embedded in CC CTMS. You can also count on experienced service and support staff that are not only attentive, but will also usually resolve your issue in the first call. The solutions are constantly evolving to meet industry trends and updates are provided at no additional cost.\n\n\nPlease contact Bio-Optronics for pricing information. Support is available via phone, email, and an online knowledge hub.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/e25282a0-2f01-47de-9f22-1469e3deaf0e.png","url":"https://www.softwareadvice.com.au/software/105345/clinical-conductor-ctms","@type":"ListItem"},{"name":"Ripple","position":16,"description":"Ripple is a web-based solution designed to manage recruitment and post-enrollment tracking of clinical trial patients. It can be used by academic institutions, contract research organizations, small medical device companies, plus more. Ripple can help clinical trial sites efficiently enroll patients, manage recruitment strategies, simplify reporting, and automate tasks.  \n\n\nThe Ripple platform includes features such as a study dashboard, patient/participant tracking, lab task management, data import/export, automated email notifications, plus more. Sites can monitor and manage participant recruitment and retention strategies using Ripple. Additionally, this solution can be used to organize patient data, access communications with contacts, and schedule upcoming appointments. \n\n\nRipple Science offers HIPAA-compliant plans and integrates with existing calendars. Please contact Ripple Science for pricing information.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/d90cb1fb-7348-48dc-9a39-be53d97b9fb5.png","url":"https://www.softwareadvice.com.au/software/105261/ripple","@type":"ListItem"},{"name":"Veeva Vault","position":17,"description":"Veeva Vault is a cloud-based content management solution with built-in collaboration features designed specifically for the life sciences industry. It comprises multiple modules that independently perform separate functions.\n\n\nVault eTMF helps life science companies manage clinical trial operations. Vault Submissions creates a single space for regulatory documents from contributors, partners, and affiliates.\n\n\nVeeva RIM provides users with an authoritative source for submission of documents, publishing dossiers, managing authority interactions, and registrations. Vault RIM also allows users to plan, manage, and track product registrations.\n\n\nVault PromoMats combines internal and external messages and creates marketing for new and existing stakeholders. Vault MedComms provides a common repository that integrates global medical communication content from all communication channels and geographies.\n\n\nFinally, Vault Investigator Portal helps sponsors and clinical research organizations maintain audit-ready eTMFs.\n\n\nUsers can raise online tickets for support inquiries.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5d8508ce-c12d-400d-9370-98d30964cdce.png","url":"https://www.softwareadvice.com.au/software/13108/veeva-vault","@type":"ListItem"},{"name":"Health Cloud","position":18,"description":"Salesforce Health Cloud is a patient management platform designed to help medium to large healthcare organizations manage inquiries, track issues, deliver post-acute care processes and more. Key features include clinical data management, event monitoring, custom care plans and team collaboration.\n\nSalesforce Health Cloud provides a 360-degree view of patients’ details and enables agents to create personalized and concurrent recovery plans, facilitating communication with caregivers in real-time. Its contact center module helps connect patients with physicians for scheduling appointments, resolving inquiries and giving care recommendations using a centralized platform. Additionally, it comes with a patient segmentation and lists module which allows users to manage tasks and assessments, improving productivity across care teams.\n\nSalesforce Health Cloud integrates with various third-party applications such as Field Service Lightning, AppExchange and Google applications. Pricing is available on monthly subscriptions and support is extended via live chat, phone and documentation.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5e707b7d-1625-4687-beb0-d7b74bc84700.png","url":"https://www.softwareadvice.com.au/software/319387/salesforce-health-cloud","@type":"ListItem"},{"name":"ClinCapture","position":19,"description":"Captivate EDC is a cloud-based electronic data capture solution that assists medical researchers and practitioners with data capture and forms management. Key features include WYSIWYG form editor, risk-based monitoring, activity dashboard, form versioning, progress tracking, and compliance management.\n\n\nThe Captivate EDC platform enables patients to fill out surveys such as pain intensity diagrams, visual analog scales, psychological symptoms, quality of life, and more. Its centralized portal enables direct collection of patient-reported outcomes, clinician outcomes, and observer outcomes. Additionally, its reporting tool allows researchers to track the progress of clinical studies in real-time as well as analyze data across studies and sites.\n\n\nCaptivate EDC comes with an application programming interface (API), facilitating integration with third-party systems such as learning management, clinical trial management, and lab management. It is available on monthly subscriptions and support is provided via phone, email, and live chat.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/ac29b954-cc7f-43b9-ba49-eb06ea0916d0.png","url":"https://www.softwareadvice.com.au/software/105231/clincapture","@type":"ListItem"},{"name":"CRIO","position":20,"description":"CRIO is a health tech company delivering comprehensive clinical research solutions for pharma, biotech, research sites, and academic research centers to streamline regulatory workflows. As the leading eSource solution for sites worldwide, CRIO’s unique architecture delivers a single point of data capture, eliminating the need for costly and delayed manual re-entry into EDC.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/31d1d7e4-fd1e-498c-b4a8-f9d396674ab9.png","url":"https://www.softwareadvice.com.au/software/307073/clinical-research-io","@type":"ListItem"},{"name":"Xolomon","position":21,"description":"Xolomon is an electronic medical record (EMR) and patient engagement solution that helps healthcare organizations streamline patient data collection and management operations from within a unified platform. It allows employees to create patient records with clinical details, such as conditions, results, and treatments. \n\nXolomon's clinical trial management module enables team members to manage tests, patient recruitment, drug administration, and other regulatory processes. Administrators can set up role-based access rights and customize the platform for multiple use cases, such as pharmaceutical, research, management, and more, whilst ensuring compliance with FDA and LOPD guidelines. Additionally, it lets staff members manage patient registration processes for hospitals, laboratories, biobanks, and medical societies. \n\nXolomon enables healthcare workers to utilize the built-in dashboard to generate personalized study reports and export data in multiple file formats. Pricing is available on request and support is extended via phone, email, documentation, and other online measures.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/7c5e3afc-de79-4078-a755-cfb5014446be.png","url":"https://www.softwareadvice.com.au/software/204376/xolomon","@type":"ListItem"},{"name":"Florence eTMF","position":22,"description":"Get set up fast with the top-rated platform in ease-of-use, ease-of-setup, and customer support. Plus, connect directly to your sites with the only eTMF integrated with the industry-standard electronic investigator site file network.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/90804cf0-6fba-4aa8-ad26-90644ec4260e.jpeg","url":"https://www.softwareadvice.com.au/software/385936/florence-etmf","@type":"ListItem"},{"name":"RegDocs365","position":23,"description":"RegDocs365 is an electronic regulatory document management (EDM) system for life sciences. It caters to biotech, pharmaceutical, and medical device companies. The platform offers core features for managing regulatory documents. It provides a centralized repository for documents like FDA 1572 forms, protocols, and SOPs. The system has robust search capabilities to find documents quickly. \n\nAdditionally, it also enables version control and audit trails to track document changes. RegDocs365 also allows for secure collaboration between internal and external users. For deployment, RegDocs365 is a cloud-based system accessed via any standard web browser. Ongoing support is provided through an expert customer service team available via phone, email, and chat.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/84402d6f-ad7c-414d-b1dd-e68182d3ec75.jpeg","url":"https://www.softwareadvice.com.au/software/249010/regdocs365","@type":"ListItem"},{"name":"STARLIMS","position":24,"description":"STARLIMS is a clinical trial management software that helps businesses collect, manage and interpret laboratory data. The platform enables managers to configure workflows for research projects and regulate compliance.\n\nAdministrators can utilize the search functionality to filter and sort data sets and analyze market trends to facilitate resource planning. Additionally, supervisors can also manage product inventory in accordance with storage capacity on a unified interface.\n\nSTARLIMS lets businesses integrate the software with existing electronic records for equipment maintenance, inventory, samples and testing schedules.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/37aedfeb-997d-4ec5-b36e-702c92df0055.png","url":"https://www.softwareadvice.com.au/software/359070/starlims","@type":"ListItem"},{"name":"Medidata CTMS","position":25,"description":"The Clinical Trial Management System (CTMS) offered by Medidata Solutions is a platform designed to enhance the efficiency and oversight of clinical studies. With features such as Rave EDC for capturing and managing patient data securely, Companion for simplifying data entry, and Site Cloud - EOS for managing clinical study files seamlessly, the CTMS improves speed and effectiveness across the trial lifecycle. It also includes tools like the Safety Gateway for automating adverse event data collection and RTSM for eliminating data entry errors in randomization and trial supply management. By using Medidata's CTMS, researchers can streamline their operations, ensure data accuracy, and drive faster timelines for successful clinical trials","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/29360d0d-1953-4b07-9908-df35533ac597.jpeg","url":"https://www.softwareadvice.com.au/software/458480/Medidata-CTMS","@type":"ListItem"}],"numberOfItems":25}
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