---
description: Discover and compare Clinical Trial Management Software Applications & Tools for Windows. Capterra is a free interactive tool that lets you quickly narrow down your software selection, contact multiple vendors, and compare platforms for your business.
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title: Clinical Trial Management Software for Windows - Price comparison & Reviews - Capterra New Zealand 2026
---

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# Clinical Trial Management Software

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> Clinical Trial Management software helps manage all aspects of clinical trials including patient data, scheduling, reporting, analysis, and data management.

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## Products

1. [Trial 360](https://www.capterra.co.nz/software/1039641/trial360) — 5.0/5 (2 reviews) — Trial 360 is a clinical trial management solution with EMR and ERP features for sites to streamline operations.
2. [MAISi](https://www.capterra.co.nz/software/142189/maisi) — 5.0/5 (1 reviews) — MAISi is a user-friendly and sophisticated Clinical Trial Management System that has been designed to assist clinical research sites.
3. [MasterControl Clinical Excellence](https://www.capterra.co.nz/software/134011/mastercontrol-clinical-suite) — 5.0/5 (1 reviews) — Software to help manage all tasks and documentation within clinical trials.
4. [Prism](https://www.capterra.co.nz/software/32514/prism) — 4.0/5 (1 reviews) — PRA Prism unifies electronic data capture, source data, and health records for clinical trial management.
5. [Phoenix CTMS](https://www.capterra.co.nz/software/175530/phoenix-ctms) — 5.0/5 (1 reviews) — Powerful open source (LGPL) CTMS/CDMS/subject registry database system, created at Medical University of Graz.
6. [Datacubed Health](https://www.capterra.co.nz/software/1020214/datacubed-health) — 4.0/5 (1 reviews) — Improve compliance and retention with actionable insights through our breakthrough patient engagement and data collection technology.
7. [TrialX](https://www.capterra.co.nz/software/1060585/trialx) — 5.0/5 (1 reviews) — Innovating in clinical research with advanced patient recruitment and remote data capture solutions for over 444 studies.
8. [ClinAsyst](https://www.capterra.co.nz/software/1090513/ClinAsyst) — 5.0/5 (1 reviews) — Cloud-based clinical trial success system (CTSS) that helps research sites streamline operations and accelerate recruitment.
9. [LifeSphere Clinical](https://www.capterra.co.nz/software/82328/agclinical) (0 reviews) — Cloud platform for clinical ops and data management that accelerates studies, ensures transparency and streamlines collaboration.
10. [CANTAB](https://www.capterra.co.nz/software/119720/cantab) (0 reviews) — Cognitive assessment and neurotechnology products accelerating clinical development.
11. [Cloudbyz CTMS](https://www.capterra.co.nz/software/146445/cloudbyz-ctms) (0 reviews) — Cloudbyz CTMS is an integrated clinical trial management solution that enables Sponsors, CRO and Sites to manage their trial operations
12. [Nucleus](https://www.capterra.co.nz/software/178268/nucleus) (0 reviews) — Nucleus - Drive your clinical trial with all of your clinical data, documents and tools in a single, secure, compliant platform.
13. [EvidentIQ eCOA](https://www.capterra.co.nz/software/1014062/evidentiq) (0 reviews) — eCOA by EvidentIQ is an intuitive and highly configurable solution that allow you to capture high quality data in clinical trials.
14. [oomnia](https://www.capterra.co.nz/software/1014310/oomnia-edcctms-system) (0 reviews) — oomnia unifies clinical research information, turning fragmented data into a structured flow across all core clinical trial systems.
15. [EvidentIQ eConsent](https://www.capterra.co.nz/software/1020681/econsent) (0 reviews) — eConsent by EvidentIQ is an intuitive end-to-end platform to digitize your Informed Consent process.
16. [ClinicalPURSUIT](https://www.capterra.co.nz/software/1024918/clinicalpursuit) (0 reviews) — ClinicalPURSUIT streamlines EDC \& CTMS activities with integrated electronic informed consent (eICF), RSTM, ePRO \& intuitive dashboards
17. [Mahalo](https://www.capterra.co.nz/software/1035980/mahalo) (0 reviews) — Mahalo is a highly customizable modern clinical trial platform that accelerates study startup, recruitment, screening, and more.
18. [EvidentIQ EDC](https://www.capterra.co.nz/software/1036959/evidentiq-edc) (0 reviews) — Clinical Data Collection Platform that allows research professionals to collect, store and manage data effectively.
19. [oomnia eTMF](https://www.capterra.co.nz/software/1029529/etmf) (0 reviews) — eTMF system for clinical teams with dashboards, audit trail, role-based access, fast setup, one login for EDC, RTSM, CTMS.
20. [StudyGen 360](https://www.capterra.co.nz/software/1061125/studygen-360) (0 reviews) — StudyGen 360 offers flexible options for study data collection and evaluation up to automated submission document creation.
21. [SiteCentric](https://www.capterra.co.nz/software/1066717/sitecentric) (0 reviews) — Clinical trial management system that allows users to manage patient recruiting, advertising and study, monitor processes, and more.
22. [Elips'PHARMA](https://www.capterra.co.nz/software/1072217/ElipsPHARMA) (0 reviews) — Elips'PHARMA is a clinical trial management software that optimizes clinical research for hospital pharmacists.
23. [oomnia eConsent](https://www.capterra.co.nz/software/1075675/oomnia-eConsent) (0 reviews) — oomnia eConsent supports both digital and paper consent, empowering patient choice and reducing consent time from weeks to minutes.
24. [oomnia eCOA](https://www.capterra.co.nz/software/1075702/oomnia-eCOA) (0 reviews) — eCOA software captures real-time patient data via devices, reducing errors through instant validation, simplifying trial workflows.
25. [oomnia CTMS](https://www.capterra.co.nz/software/1076548/oomnia-CTMS) (0 reviews) — oomnia CTMS centralizes trial data, tracks sites, manages budgets, monitors visits and automates workflows for better study control.

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## Related Categories

- [Patient Management Software](https://www.capterra.co.nz/directory/30780/patient-management/software)
- [Electronic Medical Records Software](https://www.capterra.co.nz/directory/20028/electronic-medical-records/software)
- [Workflow Management Software](https://www.capterra.co.nz/directory/30091/workflow-management/software)
- [Patient Engagement Software](https://www.capterra.co.nz/directory/31085/patient-engagement/software)
- [Appointment Scheduling Software](https://www.capterra.co.nz/directory/30757/appointment-scheduling/software)

## Links

- [View on Capterra](https://www.capterra.co.nz/directory/10035/clinical-trial-management/software)
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With single sign-on, users save up to 75% of time spent navigating between systems. Its multi-tenant design allows stakeholders to manage multiple trials on a single instance and gain oversight of entire portfolios. No coding is required due to intuitive drag-and-drop features. oomnia is fully interoperable, eliminating integration issues, and offers role-based access with a user-friendly interface customizable by language and notifications. Real-time reporting, seamless randomization, and complete audit logs enhance efficiency and data accuracy. The platform complies with 21 CFR Part 11, EU Annex 11, and CDISC standards. ISO 27001 and ISO 9001 certified and FDA/Swissmedic inspected, oomnia enables up to 50% time and cost savings through streamlined, intelligent trial management.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/c8479f5a-a481-44ff-8cfd-76bf1dec0792.png","url":"https://www.capterra.co.nz/software/1014310/oomnia-edcctms-system","@type":"ListItem"},{"name":"EvidentIQ eConsent","position":15,"description":"Looking for a way to digitize the Informed Consent process? eConsent by EvidentIQ provides you with all the tools you need! Online screening forms, eConsultation (integrated video call), eSignature and much more!\n\nEnsure better patient comprehension, achieve higher participation rates and decrease dropout rates in clinical trials. Contact our team of experts to get a free demo!","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/2a85bc1d-8dc8-4f83-8281-d6fb024316a5.jpeg","url":"https://www.capterra.co.nz/software/1020681/econsent","@type":"ListItem"},{"name":"ClinicalPURSUIT","position":16,"description":"Say goodbye to wasted time and cost building and managing clinical trials.  ClinicalPURSUIT's advanced EDC / CTMS platform allows us to rapidly set up and deploy single-center and multicenter studies in weeks. Our data management dashboards and productivity features provide HIPAA & GDP compliance with efficient workflows that simplifies data collection and study management.  Smart modules like our integrated electronic Informed Consent (eICF), and RTSM saves time and money.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/ce7b0a47-6282-49d1-8d17-c73e4a7b3b02.png","url":"https://www.capterra.co.nz/software/1024918/clinicalpursuit","@type":"ListItem"},{"name":"Mahalo","position":17,"description":"With Mahalo, you reduce the risk of patient recruitment cost overruns, patient non-adherence, high dropout rates, and severe adverse events.\n\nMahalo is the only clinical research platform to provide digital health app building blocks you can incorporate into your study or leverage to change patient behavior at scale and collect Real World Evidence (RWE) for every study.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/78c62b22-ea60-4573-8efd-9f1be765e366.png","url":"https://www.capterra.co.nz/software/1035980/mahalo","@type":"ListItem"},{"name":"EvidentIQ EDC","position":18,"description":"EvidentIQ is an innovative software solution that facilitates clinical trial data management and documentation for investigators, sites, CROs and sponsors. EvidentIQ EDC enables electronic data capture across all phases of clinical research with flexible tools allowing you to manage your site infrastructure and workflow efficiently.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/0f1bb4ef-7bcb-4f92-9fd6-16de00e18f7b.png","url":"https://www.capterra.co.nz/software/1036959/evidentiq-edc","@type":"ListItem"},{"name":"oomnia eTMF","position":19,"description":"oomnia eTMF by Wemedoo is a digital trial master file system that enables clinical teams to capture, store, manage, and track trial documentation in a secure, unified platform. Structured uploads using placeholders and automated indexing improve organization, reduce document errors, and support faster and more efficient handling. Dashboards display real-time completeness across study sites; audit trails and version control ensure traceability, support regulatory inspections, and maintain document integrity. Role-based access and encryption protect sensitive clinical data and align with GCP, EMA, ICH, GDPR, HIPAA, and ISO standards. Setup time is minimized by reusing templates, structures, roles, and user permissions across multiple studies. Single-login access integrates oomnia eTMF with EDC, RTSM, and CTMS modules, enhancing trial visibility, system access, and operational collaboration.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/60ee54a5-b2a0-4922-9621-3c687fc5e0c4.png","url":"https://www.capterra.co.nz/software/1029529/etmf","@type":"ListItem"},{"name":"StudyGen 360","position":20,"description":"StudyGen 360 offers versatile solutions for collecting, managing and analyzing study data and even automates reporting for regulatory purposes. \nAll relevant information is stored in a centralized, cloud-based repository, bypassing the limitations typical of traditional LIM systems. \nCustomized StudyGen modules meet a wide range of bioanalytical, immunogenicity, stability and archiving requirements and address specific scientific needs and challenges.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/bc823175-ddc3-4c4a-8883-1b71d2c8fc13.png","url":"https://www.capterra.co.nz/software/1061125/studygen-360","@type":"ListItem"},{"name":"SiteCentric","position":21,"description":"SiteCentric is a cloud-based clinical trial management platform designed to help all clinical research websites manage patient recruiting, generate reports, monitor patient procedures, create bills and consent forms, and more.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/1a03ea05-3137-48ad-b43a-a4aa915a45f9.jpeg","url":"https://www.capterra.co.nz/software/1066717/sitecentric","@type":"ListItem"},{"name":"Elips'PHARMA","position":22,"description":"Elips'PHARMA is a comprehensive clinical trial management software. Designed by hospital pharmacists, it optimizes clinical research through simplified administrative management. The software covers the entire clinical trial process including feasibility studies, archiving, product and inventory management, and dispensing workflows. Elips'PHARMA ensures optimal security and traceability by providing rigorous access control and detailed tracking of products and patients. Key features include trial lifecycle management, real-time traceable inventory control, secure prescription and dispensing workflows, patient data management, analytics and reporting, and advanced data protection and regulatory compliance.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/fb528fdd-6d1d-4e09-b189-d217610ff0f7.png","url":"https://www.capterra.co.nz/software/1072217/ElipsPHARMA","@type":"ListItem"},{"name":"oomnia eConsent","position":23,"description":"oomnia eConsent software by Wemedoo supports patient-centric clinical trials by digitizing informed consent. It allows participants to choose how they provide consent, including retaining the option for paper-based forms managed outside the software, based on their comfort or technology preference.\nKey features include automated multilingual consent documents, rapid digital signatures, and a built-in Q&A module enabling direct real-time communication between participants and site staff. This improves clarity and reduces delays.\nAutomatic synchronization of participant data eliminates unnecessary manual data transfers, enhancing accuracy and operational efficiency. The software connects with Electronic Data Capture (EDC) systems to support continuous trial operations. Compliance with international regulations, such as GDPR and HIPAA, is supported through strict access controls, encryption, and regular audits that ensure data security and integrity across all clinical activities.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/47205523-3085-43f0-812a-0ee38b5d0e97.png","url":"https://www.capterra.co.nz/software/1075675/oomnia-eConsent","@type":"ListItem"},{"name":"oomnia eCOA","position":24,"description":"oomnia electronic Clinical Outcome Assessment (eCOA) software by Wemedoo enables direct data collection from clinical trial participants and staff through electronic devices. This system captures patient-reported outcomes, clinician assessments, observer reports, and performance measures in real time. The technology integrates with EDC systems to centralize trial data in one database. Data validation occurs at entry, reducing errors and supporting data security and protocol compliance. Clinical teams gain immediate data access for quick analysis and decision-making. The user-friendly interface works for participants with varying levels of digital literacy. Participants use familiar devices, increasing comfort and compliance during trial reporting. The software supports small and large-scale studies with customizable forms for specific trial needs. Technical support is available during setup, data collection, and closeout to assist with system use and issue resolution.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/9d719fd8-7dc9-4e26-81af-63c58f15c8e7.png","url":"https://www.capterra.co.nz/software/1075702/oomnia-eCOA","@type":"ListItem"},{"name":"oomnia CTMS","position":25,"description":"oomnia Clinical Trial Management System (CTMS) by Wemedoo centralizes and automates the management of clinical trials from initial planning through final reporting. It integrates key trial components, including participant data, site selection, budgeting, and document management.\nDesigned as part of a unified clinical research platform, it supports data integration across modules and maintains alignment with data protection standards such as GDPR and HIPAA.\nUsers such as clinical data managers, trial directors, and research associates access real-time data on study progress, adverse events, protocol deviations, and enrollment milestones.\nBy consolidating and updating information from eCRFs, RTSM, eTMF, ePRO, and eCOA tools, CTMS reduces manual tasks, input errors, and delays, helping reduce operational costs and cycle times. The software allows tracking of expenses, participant visits, site activation status, staff training progress, and delegation records.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/dc9a7a47-6622-4bd7-aa97-22042d6bc7ba.png","url":"https://www.capterra.co.nz/software/1076548/oomnia-CTMS","@type":"ListItem"}],"numberOfItems":25}
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