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description: Page 3 - Discover the best Clinical Trial Management Software in New Zealand. Compare top Clinical Trial Management Software tools with customer reviews, pricing and free demos.
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title: Page 3 - Best Clinical Trial Management Software in New Zealand - 2026 Reviews, Pricing & Demos
---

Breadcrumb: [Home](/) > [Clinical Trial Management Software](https://www.softwareadvice.co.nz/directory/4623/clinical-trial-management/software) > [Page 3](https://www.softwareadvice.co.nz/directory/4623/clinical-trial-management/software?page=3)

# Clinical Trial Management Software

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## Products

1. [BSI CTMS](https://www.softwareadvice.co.nz/software/272614/bsi-ctms) — 5.0/5 (2 reviews) — BSI CTMS is a comprehensive software solution for clinical trial management, designed to simplify and enhance all pha...
2. [Trial 360](https://www.softwareadvice.co.nz/software/379345/trial-360) — 5.0/5 (2 reviews) — Trial 360 is a web-based FDA 21 CFR Part 11-compliant software that streamlines research site operations and improves...
3. [OmniStar Research](https://www.softwareadvice.co.nz/software/245471/omnistar-research) — 4.0/5 (1 reviews) — Research management is an ever-evolving landscape with many challenges. Time-consuming submissions and approvals slow...
4. [Datacubed Health](https://www.softwareadvice.co.nz/software/328765/datacubed-health) — 4.0/5 (1 reviews) — Designed for virtual, hybrid, or traditional clinical trial settings, our Datacubed Health App is proven to deliver 8...
5. [TrialX](https://www.softwareadvice.co.nz/software/434373/trialx-connect) — 5.0/5 (1 reviews) — TrialX simplifies the management of clinical trials for organizations through its offerings, TrialX Connect and Trial...
6. [TrialPal](https://www.softwareadvice.co.nz/software/380065/trialpal) — 4.0/5 (1 reviews) — Our eCOA/ePROfor Decentralized Clinical Trial (DCT) is the powerful TrialPal. A mobile and Web Application is an intu...
7. [Kronus](https://www.softwareadvice.co.nz/software/521109/Kronus) — 5.0/5 (1 reviews) — Kronus CTMS provides an all-in-one clinical trial management solution designed to ensure compliance and improve opera...
8. [ClinVigilant eClinical](https://www.softwareadvice.co.nz/software/439799/eclinical-suite) — 5.0/5 (1 reviews) — ClinVigilant eClinical helps streamline clinical trial management for medical professionals through its cloud-based p...
9. [Cloudbyz CTMS](https://www.softwareadvice.co.nz/software/206326/cloudbyz-ctms) (0 reviews) — Cloudbyz's Clinical Trial Management System (CTMS) is a cloud-based clinical trial operations management solution nat...
10. [Labfront](https://www.softwareadvice.co.nz/software/289529/physioq) (0 reviews) — Labfront allows researchers to access digital biomarker data from consumer wearables remotely, inexpensively, and rel...
11. [SyMetric](https://www.softwareadvice.co.nz/software/294696/symetric-c6) (0 reviews) — SyMetric is a clinical trial management solution that helps academic institutions, pharmaceutical companies and resea...
12. [TrialEngine](https://www.softwareadvice.co.nz/software/340197/r-grid) (0 reviews) — R.grid’s secure and regulation-compliant CTMS system accelerates and intelligently streamlines operations and provide...
13. [ClinicalPURSUIT](https://www.softwareadvice.co.nz/software/341632/clinicalpursuit) (0 reviews) — ClinicalPURSUIT is a clinical trial management software designed to help doctors manage patient data and monitor key ...
14. [Propel](https://www.softwareadvice.co.nz/software/333504/ignite) (0 reviews) — PROPEL is a cloud-based data analytics software that organizes and automates clinical trial pipeline management and s...
15. [TrialMaster](https://www.softwareadvice.co.nz/software/368764/trialmaster) (0 reviews) — TrialMaster is a cloud-based software designed to help medical organizations streamline clinical trial processes. Sup...
16. [EvidentIQ eCOA](https://www.softwareadvice.co.nz/software/261551/evidentiq) (0 reviews) — eCOA is an electronic clinic outcome assessment solution, which enables businesses to collect data from patients via ...
17. [EvidentIQ EDC](https://www.softwareadvice.co.nz/software/387257/evidentiq-edc) (0 reviews) — EvidentIQ EDC is a cost-effective, scalable, and compliant EDC system. EvidentIQ utilizes clinical trial software tec...
18. [EvidentIQ eConsent](https://www.softwareadvice.co.nz/software/329942/econsent) (0 reviews) — With eConsent by EvidentIQ users can digitize the entire informed consent process to make their life easier and impro...
19. [Marvin eTMF](https://www.softwareadvice.co.nz/software/228307/marvin-etmf) (0 reviews) — Marvin eTMF is a clinical trial management software designed to help businesses collect and manage documents on a uni...
20. [Trial Online](https://www.softwareadvice.co.nz/software/296278/trial-online) (0 reviews) — Trial Online is a electronic data capture solution that helps clinical trial organizations streamline processes relat...
21. [Mahalo](https://www.softwareadvice.co.nz/software/368730/mahalo) (0 reviews) — Enter Mahalo, a breath of fresh air in the world of clinical trial management. Designed with you and your patients in...
22. [Inductive EDC](https://www.softwareadvice.co.nz/software/426658/inductive-edc) (0 reviews) — Inductive EDC is a feature-rich software that enables businesses to capture, manage and report clinical trial data ac...
23. [PatienTrials](https://www.softwareadvice.co.nz/software/410951/patientrials) (0 reviews) — PatienTrials is an enterprise platform designed to accelerate clinical trial recruitment, participant engagement, and...
24. [Yunu](https://www.softwareadvice.co.nz/software/427701/yunu) (0 reviews) — Yunu is a clinical trial imaging data and workflow solution designed for cancer centers, trial sponsors, pharmaceutic...
25. [StudyGen 360](https://www.softwareadvice.co.nz/software/436057/studygen-360) (0 reviews) — StudyGen 360 adopts a centralized methodology for study data management, consolidating sample demographics, instrumen...

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BSI CTMS caters to diverse stakeholders in the clinical trial ecosystem, including pharmaceutical and biotech sponsors, diagnostics and medical device companies, contract research organizations (CROs), and academic site management organizations (SMOs).","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/f4b29b9f-38ea-44f8-af8b-07df055fe319.png","url":"https://www.softwareadvice.co.nz/software/272614/bsi-ctms","@type":"ListItem"},{"name":"Trial 360","position":2,"description":"Trial 360 is a web-based FDA 21 CFR Part 11-compliant software that streamlines research site operations and improves quality across clinical trials. Inspired by a real site network, this modular and intuitive solution is flexible and adapts to any site size, multi-site, multi-study, and multi-country organizations. \nThis integrated system is the basis for a site that complies with best practice guidelines, featuring core modules: Recruitment, Study setup, Scheduling, Electronic Medical Records (EMR), Laboratory, Pharmacy and Finance.\n\nUpgrade your site's operations faster by installing the ERP modules such as Billing, Procurement, Inventory, HR, Document management, and eLearning on an on-demand basis and with a pay-as-you-go model.\n\nTrial 360 is cost-convenient for emerging market sites and has successful experiences with vaccine studies thanks to its special features for this therapeutic area. \n\nThe software enables diversity and inclusion strategies with multiple recruiting and patient-centric communication channels.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/360c4906-89fa-4db3-ae25-22ec02e7583e.png","url":"https://www.softwareadvice.co.nz/software/379345/trial-360","@type":"ListItem"},{"name":"OmniStar Research","position":3,"description":"Research management is an ever-evolving landscape with many challenges. Time-consuming submissions and approvals slow down the research project lifecycle, and this can drastically affect innovation and progress. Thankfully, OmniStar Research is a transformative solution designed to reimagine the way research endeavours are managed. OmniStar Research is specifically designed to tackle the challenges faced by researchers and administrators alike. It reduces every manual and cumbersome task where possible in the Research Management process.\n\nSay goodbye to the maze of manual and time-consuming coordination and the frantic scramble for last-minute revisions and approvals. With OmniStar Research, research administration is collaborative and streamlined.\n\nFrom automating proposal development, tracking versions, to fostering online discussions, committee approvals, and transparent progress tracking, OmniStar makes every step of the process easy and collaborative. Whether you're teaming up on a funding proposal, handling Human, Animal & Biosafety applications, managing a committee or processing progress reports and variations, OmniStar Research streamlines the task for researchers and administrators.\n\nWe support:\n\n•\tProposal development and approval\n•\tPricing and costing\n•\tIntegration with Australian Research Council and other funders\n•\tContract and variations\n•\tHuman, Animal & Biosafety applications \n•\tVictorian Specific Module\n•\tAmendments including tracked changes \n•\tApproved animal numbers\n•\tFacility management\n•\tPre-meeting reviews and Conflict of Interest\n•\tRequest for more information\n•\tCommittee management including role management\n•\tLow and Negligible Risk and High Risk applications\n•\tDigital approvals include conditions of approval\n•\tAnnual and Final Progress Reports\n•\tAdverse Events/Safety Reports\n•\tHR and animal species integration\n•\tSingle Sign-on and MFA\n\nWHAT MAKES US DIFFERENT?\n\nImagine a future where seamless collaboration between researchers and administrators optimises research outcomes for the betterment of humanity and the planet. At OmniStar, we're not just about software; we're on a mission to transform the research management landscape. Driven by our purpose, we stand committed to simplifying the journeys of those who shape the course of the future.\n\nFrom the proposal development and collaboration, pricing and costing and integration with funders like the Australian Research Council to contract and variation management, progress reporting and digital approvals, we offer an all-encompassing solution that simplifies every step. \n\nDiscover the distinguishing features of OmniStar that set us apart:\n\n1.\tFlexibility and Configurability: Flexibility is at the front of OmniStar Research’s design philosophy. We understand that every organisation is unique. OmniStar Research is highly configurable, allowing you to tailor workflows, forms, emails and document templates to align with your specific requirements. Adapt the platform to fit your organisation's unique business processes. \n\n2.\tIntuitive User Experience: OmniStar Research boasts a user-friendly interface designed with simplicity and ease of use in mind. Researchers, reviewers, committee members and administrators can effortlessly navigate the platform.\n\n3.\tDedicated Support: Our team of experts provides exceptional customer support. From onboarding and training to ongoing assistance, we are here to ensure you extract maximum value from OmniStar Research.\n\n4.\tScalability and Adaptability: Whether you manage a small or large number of grants and research projects, OmniStar Research scales with you. As your organisation evolves and needs change, OmniStar Research adapts to meet your changing needs, ensuring a seamless management experience at every stage.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5eb7c709-8ed7-4c5a-8bf8-cc09e370c0df.png","url":"https://www.softwareadvice.co.nz/software/245471/omnistar-research","@type":"ListItem"},{"name":"Datacubed Health","position":4,"description":"Designed for virtual, hybrid, or traditional clinical trial settings, our Datacubed Health App is proven to deliver 85%+ compliance for your clinical studies. \n\nOffline data capture allows patients to remain engaged even in the absence of a wifi signal without compromising your data. Geofencing provides insights into adverse events sooner so you can keep your patients safe. \n\nOur app is rooted in behavioral science because we know that patients are the heart of everything you do. We ensure patients have the best possible experience to ensure accuracy and superior quality for your clinical studies. \n\nDiscover the Datacubed difference today!","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/7a0476c8-320a-4040-93bb-159238677507.jpeg","url":"https://www.softwareadvice.co.nz/software/328765/datacubed-health","@type":"ListItem"},{"name":"TrialX","position":5,"description":"TrialX simplifies the management of clinical trials for organizations through its offerings, TrialX Connect and TrialX Advance. These solutions streamline operations related to patient recruitment management and remote research data collection.\n\nTrialX Connect helps medical centers enhance online awareness of their trials, efficiently manage recruitment, and monitor important metrics. With features like automated trial import, customizable pre-screeners, and secure patient-investigator messaging, the platform facilitates seamless connectivity with potential participants, enabling researchers to achieve their recruitment goals.\n\nTrialX Advance facilitates remote data collection for clinical trials, enabling organizations to handle research data collection and analysis. It enables efficient remote monitoring, data collection, and analysis, reducing logistical challenges and ensuring participant convenience. Researchers can remotely gather essential data from participants, improving the overall efficiency and effectiveness of clinical trials.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/4242e5c5-466f-45aa-9a74-9a98a1e4029d.jpeg","url":"https://www.softwareadvice.co.nz/software/434373/trialx-connect","@type":"ListItem"},{"name":"TrialPal","position":6,"description":"Our eCOA/ePROfor Decentralized Clinical Trial (DCT) is the powerful TrialPal. A mobile and Web Application is an intuitive and easy-to-use tool that monitors clinical trial participants and the study through dashboards. Combined with a user-friendly interface created to generate data directly from the trial participants.\n\nThe TrialPal App is an excellent tool to enhance diversity and inclusion strategies and conduct studies in emerging markets. It has shown top adherence and reporting rates of up to 98% and high adoption in +65 population. \n\nTrialPal App easily setups for vaccine clinical trial eDiaries or surveillance forms for symptom monitoring, including subforms, grading, alerts, and AEs – SAEs real-time notifications to stakeholders, where sites can also act quickly upon receiving subject reports.\n\nTrialPal APP enables:\n- Real-time Executive Descriptive Analytics and Dashboards\n- End to End Integrations\n- Real-Time notifications\n- On-Site Patient Engagement and Site support\n- Emerging markets experience\n- Combined with Online and Self Support, and Remote Control\n- Subject Trial Pal training and follow-up\n- Customizable site reports\n- On-site and remote frequent training\n- Cell phone inventory management\n- Internet data prepaid plans management","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/849531cb-5619-4f05-8ee8-5c35e867f520.png","url":"https://www.softwareadvice.co.nz/software/380065/trialpal","@type":"ListItem"},{"name":"Kronus","position":7,"description":"Kronus CTMS provides an all-in-one clinical trial management solution designed to ensure compliance and improve operational efficiency. Centralizing management functions, it enables the organization of all aspects related to doctors, sites, schedules, and documents within a single platform. This FDA-validated system simplifies clinical trial processes, eliminating the need for multiple fragmented tools and spreadsheets. By offering a unified environment, Kronus CTMS streamlines operations, making it easier to manage essential study information, including doctors, sites, sponsors, regulators, and Institutional Review Boards (IRBs).\n\nThe platform encompasses several key features to facilitate clinical trial management. It includes master data management for seamless definition and handling of critical trial information, and document management compliance tools to maintain FDA-validated structures for Trial Master Files (eTMF) and Investigator Site Files (eISF) with controlled access and comprehensive audit trails. Patient scheduling is also enhanced through a centralized calendar interface, allowing efficient management of subject timelines and coordination across studies. Furthermore, Kronus CTMS introduces electronic patient consent capabilities for secure and compliant enrollment processes, and offers robust dashboard and analytics features for real-time data visualization and reporting. These components collectively support data-driven decision-making and optimize clinical trial outcomes.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/cd05f7cd-5e7d-466a-b36d-4472230a6e39.png","url":"https://www.softwareadvice.co.nz/software/521109/Kronus","@type":"ListItem"},{"name":"ClinVigilant eClinical","position":8,"description":"ClinVigilant eClinical helps streamline clinical trial management for medical professionals through its cloud-based platform. With a unified portal, users can easily set up trials and track patient journeys.\n\nClinVigilant eClinical's Electronic Data Capture (EDC) module enables users to create electronic case report forms (eCRFs) from paper CRFs. Our Electronic Trial Master File (eTMF) module connects sponsors, CROs, and sites, offering automated processes for managing and tracking trial documentation. Additionally, the built-in real-time monitoring ensures compliance and efficiency throughout the trial.\n\nClinVigilant eClinical comes with a patient engagement platform (eCOA, eConsent, ePRO) that lets users streamline study recruitment, screening, consent, and data collection for decentralized and hybrid research projects.\n\nEnquiries > bd (at) clinvigilant.com","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/06268fb1-1dcb-43fc-99a9-48d74c4ccbe6.png","url":"https://www.softwareadvice.co.nz/software/439799/eclinical-suite","@type":"ListItem"},{"name":"Cloudbyz CTMS","position":9,"description":"Cloudbyz's Clinical Trial Management System (CTMS) is a cloud-based clinical trial operations management solution natively built on Salesforce's platform. It enables end-to-end management across all phases of the clinical study with real-time visibility and analytics across study planning, start up, study management, and close out. Cloudbyz CTMS functionality includes:\n\n1. Study Management\n2. Projections\n3. Feasibility Survey\n4. Study Start-Up\n5. Study Budget Management\n6. Site Payments\n7. Monitoring (Central/Remote/Risk Based)\n8. eDOA\n9. Portals (Site, Sponsors and CRO)\n10. Training Management\n11. Resource Management\n12. Integration, Reports & Dashboards\n\nCloudbyz CTMS, eTMF, EDC and Safety & PV solutions are natively built on the Salesforce platform and leverage a common data model to ensure seamless integration between the systems. Additionally, users can leverage the template-based approach to accelerate their trial operations and budget processes. Its solutions span across the entire life cycle of clinical trials and help customers to stay fully compliant with global industry regulations.\n\nBenefits-\nCloudbyz provides end-to-end management of the clinical trial lifecycle, including study setup, site management, study projections, monitoring, and financial management. With Cloudbyz, you can optimize your study planning, accelerate patient recruitment, and increase trial quality, while reducing costs and minimizing risk. The solution benefits are listed below-\n\n1. Secure, reliable & scalable\n2. Faster time to value\n3. Monitor study progress & risks from planning to close-out\n4. Seamless collaboration among sponsors, CROs & sites\nImproved clinical team efficiency\n\nCloudbyz CTMS solution is designed and built to be highly scalable, secure, and reliable, providing a robust and comprehensive solution for managing clinical trial operations. Our platform is built on cutting-edge Salesforce cloud technology and is fully compliant with global regulatory standards. The cloud platform benefits are listed below-\n\n1. Real-time analytics using reports & dashboards\n2. Robust Data Security through fine-grained access control\n3. Seamless processes through workflow orchestration\n4. Scalable Data processing & storage with audit trail\n5. Ease of integration through open APIs","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/0b7d6413-d070-460d-a9b5-3f1bdc9d3720.jpeg","url":"https://www.softwareadvice.co.nz/software/206326/cloudbyz-ctms","@type":"ListItem"},{"name":"Labfront","position":10,"description":"Labfront allows researchers to access digital biomarker data from consumer wearables remotely, inexpensively, and reliably.\n\nTrack participant progress by monitoring data collection and completed tasks or questionnaires. Send push notifications to help improve adherence. \n\nObtain a broad range of physiological data including activity, sleep, heart rate, respiration, IMU, and ECG waveform.\n\nThe time-stamped data is available in easy-to-use formats and organized for quick analysis.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/e36239b1-5e27-4a88-a1f8-9c213d56ae86.png","url":"https://www.softwareadvice.co.nz/software/289529/physioq","@type":"ListItem"},{"name":"SyMetric","position":11,"description":"SyMetric is a clinical trial management solution that helps academic institutions, pharmaceutical companies and research organizations manage adaptive, umbrella and virtual clinic trials via a unified portal. The platform enables medical organizations to streamline various data management operations including designing, validation, collection, source verification and exporting. \n\nSyMetric includes subject management functionality, which allows users to handle screening, randomization, enrolments, visits, receipts, and drug dispensing activities. Additionally, it offers various features such as electronic data capture, supplies management, study versioning, medical coding, lab data management and more.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a4955883-8504-4901-9c6f-dde0c315aaa4.png","url":"https://www.softwareadvice.co.nz/software/294696/symetric-c6","@type":"ListItem"},{"name":"TrialEngine","position":12,"description":"R.grid’s secure and regulation-compliant CTMS system accelerates and intelligently streamlines operations and provides patient involvement and engagement activities. \n\nThe system can be tailored to suit the needs of different departments or organizations to maximize efficiency. With R.grid, businesses can instantly centralize workflows with automatic clinical protocol and document creation, patient anonymization, engagement, impact reporting, training, quality assurance, recruitment, communication, and stakeholder management.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/92e3d0b2-9d63-48ad-b28f-ccbbeff6b40a.png","url":"https://www.softwareadvice.co.nz/software/340197/r-grid","@type":"ListItem"},{"name":"ClinicalPURSUIT","position":13,"description":"ClinicalPURSUIT is a clinical trial management software designed to help doctors manage patient data and monitor key metrics in real-time. The platform enables managers to check, capture and store electronic data on a unified interface.\n\nAdministrators can utilize Google Maps API to enable GPS mapping of patients, sites and service providers. Additionally, ClinicalPURSUIT allows teams to analyze progress against predefined key performance indicators (KPIs) and measure assessments. Clinicians can also use pivot tables to drag and drop reporting analytics on a centralized dashboard.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/ce7b0a47-6282-49d1-8d17-c73e4a7b3b02.png","url":"https://www.softwareadvice.co.nz/software/341632/clinicalpursuit","@type":"ListItem"},{"name":"Propel","position":14,"description":"PROPEL is a cloud-based data analytics software that organizes and automates clinical trial pipeline management and study startup workflows.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/6727b565-567a-4edf-9704-f9d1107faba5.jpeg","url":"https://www.softwareadvice.co.nz/software/333504/ignite","@type":"ListItem"},{"name":"TrialMaster","position":15,"description":"TrialMaster is a cloud-based software designed to help medical organizations streamline clinical trial processes. Supervisors can identify risks and develop mitigation strategies based on key risk indicators (KRIs). \n\nTrialMaster allows organizations to access subject profiles, which helps them view various information such as safety data, medical history, vitals, and more. Clinicians can build new trials with the WYSIWYG CRF interface and access features like manual coding and auto coding. Additionally, users can generate event reports and gain insights into operational data through actionable analytics.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/59c505ca-282f-4166-b8af-754652be4512.png","url":"https://www.softwareadvice.co.nz/software/368764/trialmaster","@type":"ListItem"},{"name":"EvidentIQ eCOA","position":16,"description":"eCOA is an electronic clinic outcome assessment solution, which enables businesses to collect data from patients via assessments. \n\neCOA includes electronic data capture capabilities and instant notifications. It enables businesses to gather information from clinicians, patients and observers in compliance with several regulations.\n\neCOA integrates with various third-party platforms. Pricing is available on request and support is extended via phone and email.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/58ace177-3d4a-4abb-8e8b-340cdc73fd52.jpeg","url":"https://www.softwareadvice.co.nz/software/261551/evidentiq","@type":"ListItem"},{"name":"EvidentIQ EDC","position":17,"description":"EvidentIQ EDC is a cost-effective, scalable, and compliant EDC system.\n\nEvidentIQ utilizes clinical trial software technologies to ensure our clients receive value for money, whilst securing compliance and quality service. Our 21 CFR Part 11 compliant EDC comes with flexible features like DICOM image upload, image-based data entry, eConsent, ePRO/eDiaries (accessible via smartphone, tablet, home PC), RTSM (Randomization and Trial Supply Management) modules, MedDRA and WHODrug coding, and advanced data extraction. Easily scale and adapt our system to match any protocol for drug, device, or diagnostic studies.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/0f1bb4ef-7bcb-4f92-9fd6-16de00e18f7b.png","url":"https://www.softwareadvice.co.nz/software/387257/evidentiq-edc","@type":"ListItem"},{"name":"EvidentIQ eConsent","position":18,"description":"With eConsent by EvidentIQ users can digitize the entire informed consent process to make their life easier and improve the patient experience by meeting them online in a tailored digital environment.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/2a85bc1d-8dc8-4f83-8281-d6fb024316a5.jpeg","url":"https://www.softwareadvice.co.nz/software/329942/econsent","@type":"ListItem"},{"name":"Marvin eTMF","position":19,"description":"Marvin eTMF is a clinical trial management software designed to help businesses collect and manage documents on a unified interface. The platform enables managers to configure role-based access among staff members to record metadata and manage approval workflows.\n\nAdministrators can collect and securely store data in accordance with European medicines agency (EMA) compliance protocols. Marvin eTMF allows teams to create, update, exchange, identify and classify trial master files (TMF) in a centralized dashboard. Additionally, supervisors can utilize the drag-and-drop interface to file documents across specific locations in real-time.\n\nMarvin eTMF offers search functionality, which lets businesses locate relevant documents based on various algorithms such as file name, location, metadata, type and more. Pricing is available on request and support is extended via phone and email.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/d18e7518-9bcc-4f56-986e-01bc20e614f7.png","url":"https://www.softwareadvice.co.nz/software/228307/marvin-etmf","@type":"ListItem"},{"name":"Trial Online","position":20,"description":"Trial Online is a electronic data capture solution that helps clinical trial organizations streamline processes related to logbook management, patient communications, electronic signature capture, data storage, and more from within a unified platform. With the electronic patient reported outcome (ePRO) module staff members can configure reminders, capture multimedia data, maintain patient diaries, manage audit trails, and receive non-conformance alerts. \n\nTrial Online allows medical professionals to conduct virtual visits via the video call functionality, share images, schedule consultations, send text messages to patients, and more. Pricing is available on request and support is extended via phone, email, and other online measures.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/c67b29f0-8ceb-426c-b26a-c97f145d2bde.png","url":"https://www.softwareadvice.co.nz/software/296278/trial-online","@type":"ListItem"},{"name":"Mahalo","position":21,"description":"Enter Mahalo, a breath of fresh air in the world of clinical trial management. Designed with you and your patients in mind, Mahalo brings a modern, patient-centric approach to clinical trials. This revolutionary platform simplifies the entire process, offering a wealth of features and benefits that make it the ideal choice for anyone involved in clinical trial management, from seasoned professionals to first-time users.\n\nAt its core, Mahalo is about empowering you to create a better experience for your patients. With its innovative digital health app building blocks, you can craft a customized, user-friendly solution that supports your patients every step of the way. From microlearning tools that make complex information digestible to connected devices that enable real-time patient monitoring, Mahalo is designed to foster a true partnership between you and your patients.\n\nBut it's not just about the patients. Mahalo understands that managing a clinical trial can be a daunting task, and the platform is built to streamline every aspect of the process. Say goodbye to laborious data transcription and hello to eSource, which captures data electronically at the source and reduces data entry time by over 50%. Embrace automated appointment scheduling, allowing your patients to book appointments with just a few clicks while keeping your researchers organized and on track.\n\nThe Mahalo platform also recognizes the importance of diversity and inclusion in clinical trials. By expanding the geographic region for patient recruitment, Mahalo ensures that your study is representative of the people who will ultimately benefit from your investigational product. Additionally, the integrated Clinical Trials Management System (CTMS) enables you to gain insights into site performance, patient recruitment, and overall study progress, ensuring that you stay within budget and on schedule.\n\nAs we move towards a future where Real World Evidence (RWE) becomes a regulatory requirement, Mahalo is one step ahead. The platform offers the option to collect Real World Data (RWD), helping you stay prepared for upcoming regulatory changes and ensuring that your trial meets the highest standards of safety and effectiveness.\n\nLastly, Mahalo understands that behavior change is at the heart of many clinical trials. With its Cognitive-Behavioral Therapy (CBT) tools, you can create customized mobile apps that support patients in understanding and modifying their behaviors, leading to improved health outcomes.\n\nIn a world where clinical trial management can feel cold and impersonal, Mahalo is the warm, human touch you've been craving. It's not just about the technology - it's about creating a platform that connects you, your patients, and your researchers in a meaningful way. With Mahalo, you're not just running a trial; you're creating a community.\n\nSo, take a leap into the future with Mahalo, where clinical trials are transformed into a more efficient, patient-centric, and personalized experience. Discover the difference Mahalo can make in your clinical trial management journey today.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/78c62b22-ea60-4573-8efd-9f1be765e366.png","url":"https://www.softwareadvice.co.nz/software/368730/mahalo","@type":"ListItem"},{"name":"Inductive EDC","position":22,"description":"Inductive EDC is a feature-rich software that enables businesses to capture, manage and report clinical trial data across study phases to advance research without delays. The intuitive platform is designed to be a reliable data management ecosystem for faster study setup, improved data quality and enhanced data security. Inductive EDC is built on not just technical expertise but also decades of experience in supporting clinical trials.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/1bc22103-9429-4fa7-955e-2f71be942a5a.png","url":"https://www.softwareadvice.co.nz/software/426658/inductive-edc","@type":"ListItem"},{"name":"PatienTrials","position":23,"description":"PatienTrials is an enterprise platform designed to accelerate clinical trial recruitment, participant engagement, and study operations through an AI-powered orchestration layer that augments existing Clinical Trial Management Systems (CTMS) without requiring migration or replacement.\n\nClinical trials often rely on multiple disconnected systems including CTMS, EDC, EHR/EMR platforms, recruitment vendors, logistics providers, and site workflows. PatienTrials connects these systems through a unified digital infrastructure that enables sponsors, CROs, research sites, investigators, and participants to collaborate efficiently across the entire clinical trial lifecycle.\n\nBuilt on the ServiceNow enterprise platform, PatienTrials delivers enterprise-grade workflow automation, security, and integrations that allow organizations to modernize clinical trial operations while preserving their current technology investments.\n\nThe platform improves the participant experience while reducing the operational burden on research teams helping sponsors accelerate enrollment, improve retention, and gain real-time visibility into study performance.\n\n### Key Capabilities\n\n**AI-Powered Patient-to-Trial Matching**\nAutomatically match potential participants to relevant clinical trials using eligibility criteria and intelligent screening workflows.\n\n**Participant Engagement Platform**\nProvide participants with a digital experience that includes study information, reminders, secure messaging, and AI-powered study assistance.\n\n**Recruitment Campaign Management**\nLaunch targeted recruitment campaigns and manage participant pipelines across sites and regions.\n\n**Virtual Trial Site Capabilities**\nSupport decentralized and hybrid clinical trials through recruitment pre-screening, eConsent, ePRO/eCOA, telehealth visits, and remote monitoring.\n\n**Enterprise Integration Layer**\nIntegrate with CTMS, EDC, EHR systems, and recruitment channels to connect the clinical research ecosystem.\n\n### Benefits\n\n• Accelerate clinical trial recruitment\n• Improve participant engagement and retention\n• Reduce operational burden on research teams\n• Enable decentralized and hybrid clinical trials\n• Gain real-time visibility into recruitment performance\n\n### Who Uses PatienTrials\n\nPharmaceutical companies, biotechnology firms, CROs, clinical research sites, and patient recruitment organizations.\n\n---\n\n# Top Features\n\n• AI-powered patient-to-trial matching\n• Clinical trial recruitment management\n• Participant engagement tools\n• Recruitment pre-screening automation\n• eConsent management\n• ePRO / eCOA data capture\n• Remote patient monitoring\n• CTMS integration\n• EHR / EMR integration\n• Recruitment analytics dashboards\n\n---\n\n# Best For\n\nPharmaceutical companies, biotechnology firms, CROs, and clinical research organizations seeking to accelerate recruitment, improve participant engagement, and streamline decentralized or hybrid clinical trials while leveraging existing CTMS infrastructure.\n\n---\n\n# Why Choose PatienTrials\n\nUnlike traditional clinical trial platforms that require replacing existing systems, **PatienTrials acts as an AI-powered orchestration layer that augments CTMS and research infrastructure without migration.** Built on the ServiceNow platform, it connects sponsors, CROs, sites, and participants while enabling modern patient-centric and decentralized trial experiences.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/e3d1a268-e330-40d4-a3cb-dc0cb3074b39.png","url":"https://www.softwareadvice.co.nz/software/410951/patientrials","@type":"ListItem"},{"name":"Yunu","position":24,"description":"Yunu is a clinical trial imaging data and workflow solution designed for cancer centers, trial sponsors, pharmaceutical companies, and CROs to allow access to imaging RWD and better manage workflows.\n\nYunu is serving life science companies and cancer centers to ignite collaboration and accelerate innovation. Thousands of clinical trials rely on the platform each day, \n\n21CFR Part 11 | HIPAA | SOCII Compliant\n\n-Faster Results\n\n-Better Care\n\n-Greater Accuracy\n_____________________\n\n- Connecting and giving visibility to all sites in a trial.\n\n- All 30+ major response criteria and over 300 trial specific variants supported.\n\n- Simple onboarding for additional sites.\n\n- Leveraging a network of investigators, specialists and research sites.\n\n______________________\n\n- A single, unified trial management and patient response solution. \n\n- Real-time results and trial performance data via access controls and permission settings.\n\n- Decrease audit time and increase intelligent oversight and engagement.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/da83f2c7-f0ea-41fd-9ed5-0b40bdf64db3.jpeg","url":"https://www.softwareadvice.co.nz/software/427701/yunu","@type":"ListItem"},{"name":"StudyGen 360","position":25,"description":"StudyGen 360 adopts a centralized methodology for study data management, consolidating sample demographics, instrument data, and additional study details into a unified cloud-based data pool. Tasks like study analysis planning, run planning, data review, and analysis draw from this central data source, providing GxP reporting and non-GxP insights at the click of a button.\n\nAs a scalable, cloud-based, pay-per-use application, StudyGen 360 ensures end-to-end data integrity throughout clinical trials. The platform overcomes the limitations of traditional systems, offering a comprehensive data management approach from sample collection to the final study report. Centralize all study-related data, unlocking novel ways to analyze and compare study data based on scientific criteria and requirements over the study's duration. Tailored for Pharma, Biotech, Research, and CRO companies, StudyGen optimizes collaboration in Sponsor-CRO relationships, making it the ideal solution for streamlined and efficient clinical study management.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/bc823175-ddc3-4c4a-8883-1b71d2c8fc13.png","url":"https://www.softwareadvice.co.nz/software/436057/studygen-360","@type":"ListItem"}],"numberOfItems":25}
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