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description: Page 4 - 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: Page 4 - Best Clinical Trial Management Software - 2026 Reviews, Pricing & Demos
---

Breadcrumb: [Home](/) > [Clinical Trial Management Software](https://www.softwareadvice.com.au/directory/4623/clinical-trial-management/software) > [Page 4](https://www.softwareadvice.com.au/directory/4623/clinical-trial-management/software?page=4)

# Clinical Trial Management Software

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## Products

1. [Signals Clinical](https://www.softwareadvice.com.au/software/446822/signals-clinical) (0 reviews) — Signals Clinical revolutionizes clinical data workflows, streamlining processes and cutting down on the time spent pr...
2. [eReconciliation®](https://www.softwareadvice.com.au/software/485705/eReconciliation) (0 reviews) — eReconciliation is a software for automating high volume SAE data reconciliation, which allows for integration to dat...
3. [SiteCentric](https://www.softwareadvice.com.au/software/519925/SiteCentric) (0 reviews) — Designed to help all clinical research businesses, SiteCentric is a cloud-based clinical trial management platform th...
4. [CTMS Master](https://www.softwareadvice.com.au/software/450721/CTMS-Master) (0 reviews) — CTMS Master is a cloud-based clinical trial management system designed for organizations of all sizes, including phar...
5. [Elips'PHARMA](https://www.softwareadvice.com.au/software/524394/ElipsPHARMA) (0 reviews) — Elips'PHARMA delivers a clinical trial management solution engineered for hospital environments. Created through stra...
6. [oomnia](https://www.softwareadvice.com.au/software/496447/Oomnia-EDCCTMS-System) (0 reviews) — oomnia is a clinical data capture platform that helps businesses unify all essential clinical trial tools-EDC, RTSM, ...
7. [oomnia eCOA](https://www.softwareadvice.com.au/software/527879/oomnia-eCOA) (0 reviews) — Oomnia eCOA is an electronic clinical outcome assessment platform designed for reporting clinical trial data through ...
8. [oomnia eConsent](https://www.softwareadvice.com.au/software/527852/oomnia-eConsent) (0 reviews) — Oomnia eConsent is a digital platform designed to simplify patient onboarding and enrollment for clinical trials. It ...
9. [oomnia CTMS](https://www.softwareadvice.com.au/software/528725/oomnia-CTMS) (0 reviews) — oomnia CTMS is a clinical trial management system designed to streamline the management of clinical trials from plann...
10. [BizNET-CTM](https://www.softwareadvice.com.au/software/272357/biznet) (0 reviews) — BizNET-CTM is clinical trial management solution designed to support research processes from initiation to submission...
11. [diCELLa eCRF clinical trials](https://www.softwareadvice.com.au/software/437239/dicella-ecrf-clinical-trials) (0 reviews) — diCELLa Unlimited is a tool that enables effective clinical trial management at every stage, from trial design, throu...
12. [oomnia eTMF](https://www.softwareadvice.com.au/software/503920/eTMF) (0 reviews) — Oomnia eTMF is an electronic trial master file system designed to store and manage clinical research documentation. I...

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## Related Categories

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

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-----

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Leveraging advanced tools and innovative technologies, Signals Clinical transforms data preparation, providing users with the ability to navigate complex clinical datasets effortlessly and with maximum efficiency. Discover the power of Signals Clinical and unlock the potential to expedite clinical research and decision-making processes.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/366b3f7f-365f-4cbc-bc98-bf2048df9ebd.png","url":"https://www.softwareadvice.com.au/software/446822/signals-clinical","@type":"ListItem"},{"name":"eReconciliation®","position":2,"description":"eReconciliation is a software for automating high volume SAE data reconciliation, which allows for integration to data managemet environemnts, process redesigning, importing and comparing of SA records from clinical databases, management of operational and SAE reconciliation operations, tracking and management of audit trials and exporingg and downloading of reports.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a6007705-de5a-4a8b-94a6-a85344a89cbe.png","url":"https://www.softwareadvice.com.au/software/485705/eReconciliation","@type":"ListItem"},{"name":"SiteCentric","position":3,"description":"Designed to help all clinical research businesses, SiteCentric is a cloud-based clinical trial management platform that helps manage patient appointments, track study procedures, monitor patient advertising and more. Researchers can recruit patients by searching through databases, bulk text messaging and planning study-specific advertisements.\n\nUsers can track advertisement approvals and monitor the progress of advertisements through ROI analytics and real-time data. Users can access the study portals and all generated reports from the platform's dashboard. The platform’s eISF and eSource modules enable remote monitoring of regulatory binders and allow employees to sign documents electronically. The platform also allows users to upload files in a drag-and-drop interface and provides notifications about document updates and expiration dates.\n\nSiteCentric is offered on a monthly basis and support is extended via phone and email.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/1a03ea05-3137-48ad-b43a-a4aa915a45f9.jpeg","url":"https://www.softwareadvice.com.au/software/519925/SiteCentric","@type":"ListItem"},{"name":"CTMS Master","position":4,"description":"CTMS Master is a cloud-based clinical trial management system designed for organizations of all sizes, including pharmaceuticals, biotechnology and medical device industry, that helps conduct medical research, manage finances and tasks, generate project insights, streamline communication, create invoices and more.\n\nCTMS Master helps sponsors and contract research organizations (CROs) manage clinical research by connecting trial data sources and accessing metrics, indicators and reports. The platform offers monitoring tools and an automated site visit report (SVR) workflow that manages duplicate data entry and streamlines the creation of SVRs.\n\nCTMS Master enables businesses to maintain customizable templates for project and site documents, events, milestones and site correspondence. It allows users to generate site-specific budgets and track accrued payments and future obligations. The tool also provides project insights for clinical study projects, countries and sites.\n\nCTMS Master extends support via email and phone and pricing is available on request.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/4ce96576-59ba-47b5-873f-e32fe24813bf.webp","url":"https://www.softwareadvice.com.au/software/450721/CTMS-Master","@type":"ListItem"},{"name":"Elips'PHARMA","position":5,"description":"Elips'PHARMA delivers a clinical trial management solution engineered for hospital environments. Created through strategic partnerships with pharmacists from leading French university hospitals, the platform combines expert knowledge with practical efficiency to streamline clinical research operations.\n\nThey offer end-to-end clinical trial management, connecting every phase from feasibility studies to data archiving. The precision-driven approach guarantees complete traceability and regulatory adherence. The smart dashboard technology delivers real-time insights for informed decision-making and proactive planning.\n\nThe cornerstone of Elips'PHARMA is its inventory management system, transforming investigational drug monitoring. The solution delivers end-to-end product tracking, smart expiration date monitoring and alerts, advanced storage condition oversight, automated batch tracking system, intelligent stock level management, and real-time movement tracking.\n\nElips'PHARMA prioritizes patient care through advanced prescription and dispensing system featuring comprehensive pharmaceutical verification, smart drug interaction detection, individual dispensing protocols, multi-level safety verification, and complete pharmaceutical activity logging. The patient tracking system provides enrollment management, custom treatment monitoring, comprehensive adverse event tracking, automated scheduling system, and user-friendly monitoring interface.\n\nTeams can transform trial administration and financial tracking with smart pharmaceutical cost calculations automated cost matrix generation, live budget tracking, streamlined billing processes, and dynamic financial reporting. Elips'PHARMA provides swift navigation system adaptable dashboard interface, streamlined feature access, amart notification system, comprehensive search functionality, and intelligent analytics. Additionally, it allows operators to leverage powerful reporting tools, including automated activity reporting in-depth trial analytics, flexible performance metrics, versatile data export options, and customizable report generation.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/fb528fdd-6d1d-4e09-b189-d217610ff0f7.png","url":"https://www.softwareadvice.com.au/software/524394/ElipsPHARMA","@type":"ListItem"},{"name":"oomnia","position":6,"description":"oomnia is a clinical data capture platform that helps businesses unify all essential clinical trial tools-EDC, RTSM, CTMS, eTMF, eCOA, ePRO, and eConsent-into one cohesive system. Its multi-tenant design allows stakeholders to manage multiple trials on a single instance and gain oversight of entire portfolios. oomnia is fully interoperable and offers role-based access with a unified interface customizable by language and notifications. Real-time reporting, randomization, and complete audit logs enhance efficiency and data accuracy. The platform complies with 21 CFR Part 11, EU Annex 11, and CDISC standards.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/c8479f5a-a481-44ff-8cfd-76bf1dec0792.png","url":"https://www.softwareadvice.com.au/software/496447/Oomnia-EDCCTMS-System","@type":"ListItem"},{"name":"oomnia eCOA","position":7,"description":"Oomnia eCOA is an electronic clinical outcome assessment platform designed for reporting clinical trial data through electronic devices. It is used by pharmaceutical companies, contract research organizations, and academic institutions in clinical trials where patient-reported outcomes and clinical assessments are essential. The platform supports various therapeutic areas and study types, including medical device trials and real-world evidence studies.\n\nThe platform offers a user-friendly dashboard with mobile-first accessibility, allowing use on smartphones, tablets, and computers. It provides real-time data access and validation checks to enhance data quality. The system captures diverse data types such as structured forms, biomarkers, and sensor data, while maintaining comprehensive audit trails for traceability.\n\nOomnia eCOA adheres to regulatory standards including 21 CFR Part 11, HIPAA, GDPR, and ICH GCP. It includes automated notifications to keep studies on track and offers real-time analytics for immediate insights. Customizable forms and IoT inputs enable research teams to tailor data collection to specific study needs, ensuring consistent, high-quality data.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/9d719fd8-7dc9-4e26-81af-63c58f15c8e7.png","url":"https://www.softwareadvice.com.au/software/527879/oomnia-eCOA","@type":"ListItem"},{"name":"oomnia eConsent","position":8,"description":"Oomnia eConsent is a digital platform designed to simplify patient onboarding and enrollment for clinical trials. It ensures secure processes and regulatory compliance, serving clinical research organizations, pharmaceutical sponsors, and academic institutions. The platform is beneficial for medical device trials, real-world evidence studies, and decentralized clinical trials due to its streamlined consent management capabilities.\n\nThe system includes advanced digital signature technology that supports complex workflows and multi-signature processes with complete traceability. Participants can access consent forms in their native language from any device, with support for over twenty languages to enhance global accessibility. It offers both digital and paper consent options, along with interactive multimedia elements such as videos and question-answer sections to improve participant understanding. Real-time notifications alert staff to incomplete processes, helping trials run smoothly and on schedule.\n\nOomnia eConsent integrates with Electronic Data Capture systems and Clinical Trial Management Systems, creating efficient workflows and reducing manual data entry. The platform generates customizable reports with role-based access controls, providing insights while maintaining audit-ready documentation. Security measures include encryption and strict access controls to protect sensitive patient information. The system complies with regulatory standards such as CFR Part 11, HIPAA, GDPR, and ICH GCP, ensuring data integrity throughout the consent process.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/47205523-3085-43f0-812a-0ee38b5d0e97.png","url":"https://www.softwareadvice.com.au/software/527852/oomnia-eConsent","@type":"ListItem"},{"name":"oomnia CTMS","position":9,"description":"oomnia CTMS is a clinical trial management system designed to streamline the management of clinical trials from planning to completion. It serves as a centralized platform for research organizations, pharmaceutical companies, and clinical research organizations. The system enhances efficiency and maintains regulatory compliance throughout the clinical trial lifecycle. It provides real-time access to clinical data, benefiting both small research teams and large multinational trial operations.\n\nThe system includes study planning tools such as site selection, investigator tracking, and milestone management for efficient trial setup. oomnia CTMS offers monitoring capabilities with training management, visit scheduling, participant progress tracking, and adverse event monitoring. It includes financial management tools for budget creation and invoice processing, along with customizable reporting and real-time data visualization. Security measures include role-based access control and detailed audit trails to ensure data integrity and regulatory compliance.\n\noomnia CTMS operates as a unified system that integrates with various clinical research tools. Its modular flexibility allows adaptation to evolving trial needs. The platform combines clinical expertise with automation technologies to reduce manual work and streamline workflows. This approach provides stakeholders with immediate access to critical trial information for effective decision-making throughout the clinical research process.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/dc9a7a47-6622-4bd7-aa97-22042d6bc7ba.png","url":"https://www.softwareadvice.com.au/software/528725/oomnia-CTMS","@type":"ListItem"},{"name":"BizNET-CTM","position":10,"description":"BizNET-CTM is clinical trial management solution designed to support research processes from initiation to submission. It is used by organizations such as contract research organizations, pharmaceutical companies, biotech firms, and medical device industries. The solution helps businesses accommodate various trial phases, including early phase, late phase, oncology trials, registry trials, and post approval trials.\n\nThe system includes electronic data capture features with audit trails and compliance with CDISC SDTM standards to ensure data integrity. It enables teams to support volunteer enrollment using iris recognition technology. The platform provides electronic case record form functionality with reusable templates and an interface designed for efficient study setup. It facilitates planning, managing, designing, executing, monitoring, and analyzing trial activities while adhering to protocols and regulatory requirements.\n\nBizNET-CTM is validated to meet 21 CFR Part 11 and Annex 11 GCP guidelines, ensuring compliance with regulatory standards. It offers real-time data access for tracking and managing studies throughout the lifecycle. The system includes a BioLyte component for bioanalytical laboratory automation to streamline workflows.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/58bd9dff-7715-4230-9fe4-683d42b58001.png","url":"https://www.softwareadvice.com.au/software/272357/biznet","@type":"ListItem"},{"name":"diCELLa eCRF clinical trials","position":11,"description":"diCELLa Unlimited is a tool that enables effective clinical trial management at every stage, from trial design, through data collection and patient safety management, to trial documentation management and monitoring the activities of all parties involved in the clinical trial process.\n\ndiCELLa Unlimited has integrated eCRF and CTMS modules.\n\nThe application is focused on the needs of the Sponsor/CRO and the research team. \n\nOur system offers all the necessary modules:\n1. eCRF with remote monitoring module\n2. CTMS\n3. IWRS/RTSM, \n4. SAFETY: AE/SAE Tracking, Safety Management\n5. CTMS interated with eCRF\n5.a. patients management\n5.b. sites management\n5.c. SOP development\n5.d. Agreements management\n5.e. Team activities and working time/trip reporting\n6. Query analysis\n7. Finances, Budget Management and invoicing\n8. eTMF/eISF\n9. ePRO\n10. Central Imaging Lab.\n\nKey Features:\n1. All types of randomization\n2. Defined randomization procedures\n3. Real-time randomization status tracking\n4. Defined procedures for reporting adverse events\n5. Management from the level of site, CRO and sponsor\n6. Defining IMP management procedures\n7. Track deliveries, shipments, allocations, inventory and assignments\n8. Management of entities related to the clinical trial\n9. The possibility of creating different categories of entities\n10. The ability to assign a subcontractor to various projects\n11. Knowledge management in the organization\n12. All projects in one platform\n13. CTMS REAL TIME DATA 100% integration with eCRF\n14. Overview of all clinical trials at the site, quick access to trial results in the specific site\n15. List of all patients from all sites in the clinical trial\n16. Analysis of the completion status in the eCRF\n17. Recruitment progress statistics\n18. Query response analysis\n19. SOP management\n20. Remote monitoring.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/f654867f-ea1a-4a53-9622-d3dd56ecb153.png","url":"https://www.softwareadvice.com.au/software/437239/dicella-ecrf-clinical-trials","@type":"ListItem"},{"name":"oomnia eTMF","position":12,"description":"Oomnia eTMF is an electronic trial master file system designed to store and manage clinical research documentation. It serves clinical research organizations, pharmaceutical companies, and academic institutions conducting various types of clinical trials, including medical device trials, real-world evidence studies, and traditional clinical trials.\n\nThe system provides real-time inspection readiness with live tracking and instant document retrieval. It features intuitive interfaces for quick uploads, reviews, and approvals, facilitating communication among sponsors, sites, and CROs. Oomnia eTMF ensures document security and integrity with role-based access control, data encryption, and two-factor authentication. It includes automated document indexing, categorization, and version control, along with comprehensive audit trails to track system changes.\n\nOomnia eTMF complies with regulatory requirements such as 21 CFR Part 11, HIPAA, GDPR, ICH GCP, and Swiss Data Privacy Law. It offers real-time dashboards displaying completeness metrics and document status to keep trial documentation audit-ready. Users can export data in CSV, XLSX, and XML formats for efficient handling and report generation. The platform supports the CDISC TMF Reference Model and guidelines such as ISO 14155:2020, making it adaptable to different documentation standards.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/60ee54a5-b2a0-4922-9621-3c687fc5e0c4.png","url":"https://www.softwareadvice.com.au/software/503920/eTMF","@type":"ListItem"}],"numberOfItems":12}
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