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description: Page 2 - 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 2 - Best Clinical Trial Management Software - 2026 Reviews, Pricing & Demos
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# Clinical Trial Management Software

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## Products

1. [Datacapt](https://www.softwareadvice.com.au/software/252355/datacapt) — 4.7/5 (16 reviews) — Datacapt provides a global, intuitive, flexible, and affordable electronic data capture platform with eCRF, ePRO, eCO...
2. [StudyPal](https://www.softwareadvice.com.au/software/472165/StudyPal) — 3.9/5 (15 reviews) — Delve Health is a clinical trial compliance and patient engagement company. We combine eCOA/ePRO, wearable device int...
3. [Medicai](https://www.softwareadvice.com.au/software/371369/medicai) — 4.9/5 (14 reviews) — Medicai is a cloud-based PACS and medical imaging platform designed to help radiologists, specialists, and care teams...
4. [Clinion EDC](https://www.softwareadvice.com.au/software/257516/clinion-edc) — 4.5/5 (14 reviews) — An award-winning, AI-native Electronic Data Capture platform Clinion EDC is built on a native AI foundation, enabling...
5. [Agatha Applications](https://www.softwareadvice.com.au/software/354908/agatha-clinical) — 4.6/5 (14 reviews) — Agatha Applications is a suite of web-based applications that help biotech and pharmaceutical companies manage their ...
6. [Flex Databases platform](https://www.softwareadvice.com.au/software/456034/Flex-Databases-platform) — 4.5/5 (13 reviews) — Flex Databases provides software for businesses in the life science industry to manage trials, documents, quality, an...
7. [Jeeva eClinical Cloud](https://www.softwareadvice.com.au/software/267792/jeeva-eclinical-cloud) — 4.8/5 (12 reviews) — Jeeva eClinical cloud helps clinical researchers, Biotech sponsors, and CROs accelerate remote patient recruitment. T...
8. [Prelude EDC](https://www.softwareadvice.com.au/software/109629/vision) — 5.0/5 (12 reviews) — Designed for clinical research, Prelude EDC is a CFR, Annex 11, and HIPAA compliant EDC solution that streamlines the...
9. [AQ Platform](https://www.softwareadvice.com.au/software/425761/aq) — 4.8/5 (12 reviews) — Run inspection-ready research without chasing documents across spreadsheets, shared drives and email. AscensionQ (AQ ...
10. [UnitusTI](https://www.softwareadvice.com.au/software/356587/unitusti) — 4.9/5 (9 reviews) — For service-based professionals of many disciplines, UnitusTI is a HIPAA/FERPA/GDPR-compliant, cloud-based, and encry...
11. [CRFweb](https://www.softwareadvice.com.au/software/289392/crfweb) — 4.8/5 (8 reviews) — Clindox's integrated EDC application, CRFWEB, is the perfect tool for your clinical research needs. It offers eCRF, e...
12. [Florence SiteLink](https://www.softwareadvice.com.au/software/371237/sitelink) — 4.8/5 (6 reviews) — SiteLink facilitates automated workflows like electronic logs, placeholders, eSignatures and quality assurance workfl...
13. [Dacima Clinical Suite](https://www.softwareadvice.com.au/software/130804/dacima-clinical-suite) — 5.0/5 (5 reviews) — Dacima Clinical Suite is a cloud-based electronic data capture (EDC) and study management (CTMS) system designed to s...
14. [RAYLYTIC Platform](https://www.softwareadvice.com.au/software/207481/unity) — 4.8/5 (5 reviews) — UNITY is a cloud-based solution that helps clinics manage the collection of clinical data, recording of patient-repor...
15. [MainEDC](https://www.softwareadvice.com.au/software/146437/mainedc) — 4.8/5 (5 reviews) — Complex eClinical Solution for EDC/ERT/eCOA that significantly speeds up the start of clinical trials (up to 5 days),...
16. [ARCS](https://www.softwareadvice.com.au/software/210223/arcs) — 5.0/5 (5 reviews) — ARCS is a cloud-based panel management solution that helps research institutions schedule study sessions, manage part...
17. [Studypages](https://www.softwareadvice.com.au/software/524873/Studypages) — 5.0/5 (5 reviews) — Studypages is a clinical research platform that unifies the participant experience and clinical operations. It provid...
18. [StudyTeam for Sites](https://www.softwareadvice.com.au/software/250592/studyteam) — 4.8/5 (5 reviews) — StudyTeam for Sites is a user-friendly clinical trial management system designed for clinical research sites. Sites c...
19. [Nuvertos](https://www.softwareadvice.com.au/software/383718/nuvertos) — 5.0/5 (4 reviews) — NuvertOS is a healthcare management solution that helps hospitals, clinics, and more with managing health records, bi...
20. [DFdiscover](https://www.softwareadvice.com.au/software/265272/dfdiscover) — 5.0/5 (3 reviews) — DFdiscover is a cloud-based electronic data capture solution that allows healthcare organizations to streamline clini...
21. [WeGuide](https://www.softwareadvice.com.au/software/519063/WeGuide) — 4.7/5 (3 reviews) — WeGuide is a web-based digital health platform that simplifies clinical trials and research studies by providing eScr...
22. [Ennov CTMS](https://www.softwareadvice.com.au/software/311880/ennov-ctms) — 2.0/5 (2 reviews) — Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficien...
23. [Encapsia](https://www.softwareadvice.com.au/software/105252/encapsia) — 5.0/5 (2 reviews) — Encapsia is a clinical data suite designed to help organizations streamline capturing, management, and reporting of e...
24. [iMednet](https://www.softwareadvice.com.au/software/138547/imednet) — 5.0/5 (2 reviews) — iMednet is a cloud-based electronic data capture platform designed to help the healthcare industry capture, clean, ad...
25. [Complion](https://www.softwareadvice.com.au/software/301547/complion) — 4.5/5 (2 reviews) — Designed for hospitals, medical centers, trial sites and more, Complion is a cloud-based clinical trial management so...

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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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Datacapt brings simplicity, efficiency, and quality to the collection of clinical data.\n\nDatacapt is making the promise to simplify and accelerate clinical trials with innovative tools.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/1188ad32-b7cb-4679-93d8-84e5c47ea0f7.png","url":"https://www.softwareadvice.com.au/software/252355/datacapt","@type":"ListItem"},{"name":"StudyPal","position":2,"description":"Delve Health is a clinical trial compliance and patient engagement company. We combine eCOA/ePRO, wearable device integration, real-time analytics, and Concierge-as-a-Service™ to help sponsors, CROs, and research sites run studies with higher completion rates, stronger retention, and cleaner data. Based in Minneapolis, serving programs across North America, Europe, Asia, and MENA.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5c814b00-e22e-4ab2-af23-e1667cc6822c.png","url":"https://www.softwareadvice.com.au/software/472165/StudyPal","@type":"ListItem"},{"name":"Medicai","position":3,"description":"Medicai is a cloud-based PACS and medical imaging platform designed to help radiologists, specialists, and care teams work faster and collaborate more effectively. It brings AI-assisted reporting, structured templates, case-based collaboration, and secure medical imaging exchange into one unified workspace—accessible from any device.\n\nWith Medicai, imaging studies can be uploaded directly from PACS, modalities, CDs, or a web browser, and are instantly available in a browser-based DICOM Viewer. No local installation, VPN, or workstation configuration is required. The viewer supports multi-series comparison, synchronized windows, measurements, annotations, and multi-modality workflows including MRI, CT, PET-CT, Ultrasound, and X-ray.\n\nMedicai’s AI Copilot assists radiologists with summarization, voice-guided dictation, and structured reporting. This helps standardize terminology, reduce turnaround times, and maintain reporting quality across providers, shifts, and locations.\n\nAll imaging, documents, notes, messages, and reports are organized into shared patient case timelines. Specialists, surgeons, referring physicians, or legal teams can be invited securely into cases with granular access control and complete audit trails. Patients can upload their own imaging using secure upload links, eliminating CDs and manual transfers.\n\nFor multi-site organizations and teleradiology networks, Medicai supports workload routing, case assignment, queue visibility, and quality assurance review. Video consultations—either via integrated calls or Zoom—can be launched directly inside a case for live diagnostic discussions. This enables remote reading workflows, multi-disciplinary collaboration, tumor boards, and second opinions without switching tools.\n\nKey Capabilities\n\t•\tCloud PACS with encrypted, scalable storage\n\t•\tBrowser-based DICOM Viewer with no local software required\n\t•\tAI-assisted structured reporting and voice dictation\n\t•\tCase-based collaboration and messaging\n\t•\tRole-based access controls and HIPAA/GDPR compliance\n\t•\tSecure patient and referring physician upload links\n\t•\tWorklist management for multi-site radiology groups\n\t•\tSupport for remote reading, hospital networks, and growing imaging operations\n\nWho Medicai is Built For\n\t•\tRadiology groups and teleradiology providers\n\t•\tImaging centers and diagnostic clinics\n\t•\tHospitals and healthcare networks\n\t•\tMulti-specialty practices that coordinate across locations\n\t•\tOncology boards, orthopedic teams, cardiology networks, OB/GYN care, neurology specialists\n\t•\tLegal teams and case review networks working with medical evidence\n\nCommon Use Cases\n\t•\tCloud PACS replacement or modernization\n\t•\tFaster diagnostic reporting with AI support\n\t•\tRemote/hybrid radiology workflows\n\t•\tImage sharing with referring physicians and specialists\n\t•\tPatient imaging upload and portal access\n\t•\tSecond opinions and inter-physician collaboration\n\t•\tTumor boards and multi-disciplinary case discussions\n\t•\tPI law case evaluation and medical evidence sharing\n\nMedicai delivers the flexibility of cloud access while maintaining medical-grade security and regulatory compliance. It streamlines imaging workflows, reduces reliance on CDs and manual file transfers, and enables radiologists and care teams to collaborate in real time—anywhere.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a3158696-05d4-41fb-8c72-9a3dc3b7efec.jpeg","url":"https://www.softwareadvice.com.au/software/371369/medicai","@type":"ListItem"},{"name":"Clinion EDC","position":4,"description":"An award-winning, AI-native Electronic Data Capture platform\nClinion EDC is built on a native AI foundation, enabling faster study builds, more efficient data review, and quicker database lock. As part of a unified eClinical platform, it ensures seamless data flow across modules while maintaining high standards of data quality and compliance.\n\nKey Capabilities\n● Accelerated Study Setup with Standardized Libraries\nConfigure and deploy studies in weeks using prebuilt, CDASH-compliant templates. Remove manual programming with a flexible, codeless setup.\n● AI-Driven Data Review and Discrepancy Detection\nAI reads protocol and CRF context to identify discrepancies and generate queries directly within the EDC, reducing manual review effort.\n● Real-Time Mid-Study Changes\nApply protocol amendments without downtime. Update forms or visits in live studies with automatic version control and no data loss.\n● AI-Powered Reporting\n Generate custom reports using natural language inputs. Maintain audit trails and automate report sharing without coding.\n● Automated CDISC/CDASH Mapping\nMap variables to standards within minutes using AI-assisted suggestions, reducing manual effort and supporting compliance.\n● AI Assistant for In-Platform Support\nAccess instant guidance through a conversational assistant trained on study protocols and system workflows.\n● Unified Platform with Seamless Integration\nWorks natively with RTSM, ePRO, CTMS, eConsent, and eSource, ensuring consistent data across the study lifecycle.\nImpact\n1–2 week average study go-live timeline\n40–50% faster database lock\nUp to 50% reduction in study build effort\nReduced manual queries and review cycles","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a853574d-0f1b-4990-8708-92bcb0ca3c16.png","url":"https://www.softwareadvice.com.au/software/257516/clinion-edc","@type":"ListItem"},{"name":"Agatha Applications","position":5,"description":"Agatha Applications is a suite of web-based applications that help biotech and pharmaceutical companies manage their processes. The Agatha Applications suite includes contract management, project management, CRF management and electronic signature capabilities that allow users to efficiently manage the full biopharmaceutical development lifecycle.\n\nRemote ISF enables sponsors and CROS to remotely monitor sites and study documentation. It is a secure, cloud-based system with password-protected access that allows users to view study documents, receive alerts and updates on completed tasks, and flag issues which require attention.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/f15a2f90-f424-4c79-b457-b143b3c8fadc.jpeg","url":"https://www.softwareadvice.com.au/software/354908/agatha-clinical","@type":"ListItem"},{"name":"Flex Databases platform","position":6,"description":"Flex Databases provides software for businesses in the life science industry to manage trials, documents, quality, and people. The system includes CTMS Software, eTMF, document management system, project management, budgeting, pharmacovigilance software, quality management, and learning management systems.\n\nIt offers a platform which allows combining traditional features related to management of clinical trials with the functionality for running internal pharma companies and CRO processes as well as a capability to manage financial data, invoicing and expenses. All modules developed by Flex Databases are validated and compliant with 21 CFR Part 11 and ICH GCP, and other global regulations.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/2156f2c1-3cf3-4756-946f-e32f666f6db4.png","url":"https://www.softwareadvice.com.au/software/456034/Flex-Databases-platform","@type":"ListItem"},{"name":"Jeeva eClinical Cloud","position":7,"description":"Jeeva eClinical cloud helps clinical researchers, Biotech sponsors, and CROs accelerate remote patient recruitment. The software offers a flexible bring your own device (BYOD) SaaS solution that works on any type of browser enabled mobile device & can save more than 70% time and logistical issues on patients or study teams. It was specifically designed with as a modular software, allowing for study configurations with the features and workflows that fit specific short-term or long-term trial protocols. It can be used for cross-sectional or longitudinal, observational or for  interventional studies.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/48d64543-ef6e-4ffb-86ea-bbc5def53837.jpeg","url":"https://www.softwareadvice.com.au/software/267792/jeeva-eclinical-cloud","@type":"ListItem"},{"name":"Prelude EDC","position":8,"description":"Designed for clinical research, Prelude EDC is a CFR, Annex 11, and HIPAA compliant EDC solution that streamlines the data collection process, automates data cleaning efforts, and monitors the state of electronic case reports forms (eCRFs). Prelude EDC cuts down on operational flows and reduces user-errors for clinical trials using inventory management, invoicing, and document management functionality, while also providing high-level data visibility using quick filters and data aggregation tools. \n\n\nAs a data collection solution, Prelude EDC allows users to capture digital information with unlimited rows using standard data entry elements such as text fields, radio buttons, drop-downs, and checkboxes or with custom data entry elements such as VAR scales and interactive charts. Users can utilize powerful edit checks to confirm that all data is collected for eCRFs and meets form requirements. Built-in data indicators are able to identify the state of eCRFs and focus on forms that are in-progress and forms that display errors.\n\n\nFor patient-reported outcomes, Prelude provides a mobile app, Prelude ePRO, that enables patients to input data directly for an easy and efficient experience.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/ae898a9a-b73c-4c28-83e9-2632d1248d57.png","url":"https://www.softwareadvice.com.au/software/109629/vision","@type":"ListItem"},{"name":"AQ Platform","position":9,"description":"Run inspection-ready research without chasing documents across spreadsheets, shared drives and email.\n\nAscensionQ (AQ Trials) is a connected clinical-research platform for CROs, biotech, pharma sponsors, research sites and academic institutions. It unifies your electronic Investigator Site File (eISF), electronic Trial Master File (eTMF), electronic Pharmacy Site File (ePSF), CTMS, delegation of authority, CAPA, quality management (QMS), reporting, version control and multi-site oversight in one inspection-ready environment, so the people who do the work spend less time filing and more time delivering trials.\n\nMost point tools digitise the binder and stop there. AscensionQ turns the site file into a live control layer. Frontline teams work in a simple, role-based view: find the current protocol, sign a delegation entry, return a document in seconds. Meanwhile sponsors, CRAs and governance leads get real-time visibility of what is filed, signed, overdue and at risk, across every study, site and country, with no separate trackers to maintain.\n\nEngineered against the standards inspectors expect worldwide, AscensionQ is built to ICH-GCP E6(R3), 21 CFR Part 11, ALCOA++, EMA computerised-systems expectations and GxP / GAMP 5, with ISO 27001 / 22301 alignment and an information-governance evidence pack available for technical review. It is tried and tested in live NHS research, from single-site adoption at Liverpool University Hospitals to a 300+ user QMS and CAPA deployment co-developed with the Royal Free, proven in one of the world's most demanding regulatory environments.\n\nWhy teams choose AscensionQ\n\nOne connected platform, not a stack of point tools: eISF, eTMF, ePSF, CTMS, delegation, CAPA, QMS and reporting in one place, with a single audit trail.\nAdoption-first, built by researchers, for researchers: a clean working view for frontline teams, with oversight generated automatically from the work they already do.\nInspection-ready by design: current documents, approvals, e-signatures, delegation records and CAPAs always live and linked, visible on screen rather than rebuilt site by site.\nNative pharmacy control (ePSF): pharmacy files, IP accountability and dispensing records inside the same governed environment.\nBuilt for multi-site and multi-country programmes: role-based access, site and trial segregation and central document control, with sponsor and hub visibility of readiness across every site.\nModules\n\neISF 2.0: structured folders and templates, version control, e-signature, delegation records and a live readiness view.\neTMF and ePSF: trial master file and native pharmacy site file, with templates by study and site, IP accountability, approvals and granular access by role.\nCTMS: study and site management, milestones, monitoring visits, enrolment metrics and budget tracking.\nDelegation of Authority: signed, version-controlled delegation logs and authority records, linked to training and roles.\nCAPA management: turn a document or quality issue into a logged deviation, corrective action, preventive action and resolution trail.\nQuality management (QMS): controlled SOPs and documents, training records and quality workflows linked to CAPA.\nReporting: configurable dashboards and exports across studies, sites, documents and quality metrics.\nMulti-site oversight and Study Command Centre: a readiness view of document status, signatures, overdue and at-risk items, plus a cross-site readiness grid.\nConfigured to your operating model, with hub-and-spoke document distribution, pharmacy hub flow and inspection-readiness scoring.\n\nWho it is for\nCROs, biotech and pharma sponsors, research sites and site networks, academic and non-commercial research institutions, R&D and quality teams, clinical operations and trial managers, and clinical trials pharmacy teams.\n\nStop rebuilding inspection readiness site by site. Book a 30-minute demo and we will walk it through against the way your team actually works.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/60305165-ddb1-4b27-9cf8-afc0f910e5c0.png","url":"https://www.softwareadvice.com.au/software/425761/aq","@type":"ListItem"},{"name":"UnitusTI","position":10,"description":"For service-based professionals of many disciplines, UnitusTI is a HIPAA/FERPA/GDPR-compliant, cloud-based, and encrypted practice management system. UnitusTI is multidisciplinary and can be used for ABA therapy, music therapy, speech therapy, occupational therapy, life coaching, residential care, school districts, occupational therapy, and more. Teams can use UnitusTI with the existing curriculum or program. UnitusTI delivers assessments, programs, materials, curricula, virtual materials, calendars, session notes, and practice management.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/48afe067-ddf3-4d00-8e67-e005c213e25f.png","url":"https://www.softwareadvice.com.au/software/356587/unitusti","@type":"ListItem"},{"name":"CRFweb","position":11,"description":"Clindox's integrated EDC application, CRFWEB, is the perfect tool for your clinical research needs.\n\nIt offers eCRF, eDiary, and ePRO functionality plus integrated Randomization and MedDRA coding modules.\n\nWith this software, you can eliminate redundant data entry by using one platform for all of your clinical trial requirements. The integration of these features into one comprehensive tool streamlines the workflow of your clinical trials by automating many activities that have traditionally required manual entry, including:\n\n- Automated data entry\n\n- Data validation checks\n\n- Automatic data quality assurance reports\n\n- Exports to external databases","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/6940bfb5-b720-42f5-b425-acda9bcba10a.png","url":"https://www.softwareadvice.com.au/software/289392/crfweb","@type":"ListItem"},{"name":"Florence SiteLink","position":12,"description":"SiteLink facilitates automated workflows like electronic logs, placeholders, eSignatures and quality assurance workflows, reduces start-up times by 40% for most of our customers and accelerates overall study timelines to reduce time to submission.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/e3a8aa20-6a06-4904-b672-87833f772aa8.jpeg","url":"https://www.softwareadvice.com.au/software/371237/sitelink","@type":"ListItem"},{"name":"Dacima Clinical Suite","position":13,"description":"Dacima Clinical Suite is a cloud-based electronic data capture (EDC) and study management (CTMS) system designed to streamline clinical trial data collection processes. This solution includes interactive dashboards, a CDISC-compliant form library, and detailed reporting functions. With built-in, interactive dashboards, users can access and filter data by several metrics, including subject recruitment, audit trail events, status tracking, summary statistics, plus more.\n\n\nWith Dacima Clinical Suite, administrators can manage user permissions by creating users and user groups with delegated access to studies, sites, forms, dashboards, plus more. Additionally, clinical trial teams can access monitoring, web survey, and patient diary tools. Other Dacima solution options that can be added to this suite include a Randomization Module (IWRS), Drug Supply Management module, Electronic Patient-Reported Outcome (ePRO) module.\n\n\nDacima Clinical Suite integrates with Rybbon Digital Gifting, Salesforce, plus more. Support is available via phone and online methods. Please contact Dacima for pricing information.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/fc3e4844-815d-4ba9-9651-b24a370a9125.png","url":"https://www.softwareadvice.com.au/software/130804/dacima-clinical-suite","@type":"ListItem"},{"name":"RAYLYTIC Platform","position":14,"description":"UNITY is a cloud-based solution that helps clinics manage the collection of clinical data, recording of patient-reported outcomes, extraction of radiographic data and other related operations The platform assists administrators with planning, monitoring, and analysis of clinical trials or post-market monitoring studies. \n\nUnity lets organizations digitize, automate, and standardize routine processes via real-time reports. It offers a host of features such as automated alerts, dashboards, risk-based monitoring, overviews and more.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/edebfeb2-cc9c-4770-8884-eb19ced9ac7a.jpeg","url":"https://www.softwareadvice.com.au/software/207481/unity","@type":"ListItem"},{"name":"MainEDC","position":15,"description":"Complex eClinical Solution for EDC/ERT/eCOA that significantly speeds up the start of clinical trials (up to 5 days), saves budget (up to 80% for monitoring), increases the capitalization and attractiveness of your company (noted by 89% of customers). Increases the knowledge and advancement of Data Management and Data Science professionals (noted by 96% of specialists). 94% of investigators like the usability of interfaces.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/549eadc3-6cbf-4b9c-adc7-99693860ef37.png","url":"https://www.softwareadvice.com.au/software/146437/mainedc","@type":"ListItem"},{"name":"ARCS","position":16,"description":"ARCS is a cloud-based panel management solution that helps research institutions schedule study sessions, manage participants and streamline other administrative processes. Professionals can use the dashboard to schedule appointments on a calendar and track the progress of sessions via actionable analytics.\n\nARCS allows organizations to build personalized profiles for members with information, such as contact details, eligibility verification and more. Managers can assign questionnaires to specific participants, view comments and send updates via SMS. Additionally, it lets users create custom incentive programs with gift cards or reward points to improve participants’ overall experience.  \n\nARCS enables institutions to integrate the platform with Twilio and DocuSign, helping them capture members’ signatures across forms. Pricing is available on monthly subscriptions and support is extended via documentation and other online measures.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/5ec1f5ab-dc4f-4ab3-8ab5-650292a945e3.png","url":"https://www.softwareadvice.com.au/software/210223/arcs","@type":"ListItem"},{"name":"Studypages","position":17,"description":"Studypages is a clinical research platform that unifies the participant experience and clinical operations. It provides a single integrated platform for research organizations to conduct clinical research. Studypages caters to sponsors, sites and participants involved in clinical trials across various industries such as pharmaceuticals, biotechnology and medical devices.\n\nThe platform offers tools to engage, communicate and collaborate with participants and research sites. These include study listings and galleries, participant tracking and management, secure chat and calls as well as features for teamwork and organization. \n\nIts intelligent workflow platform helps remove trial participation barriers, making it easier for research sites to manage clinical operations. Studypages facilitates efficient conduct of clinical trials and participant engagement.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/7f266488-0b9f-48bd-8564-5cb13dd75626.jpeg","url":"https://www.softwareadvice.com.au/software/524873/Studypages","@type":"ListItem"},{"name":"StudyTeam for Sites","position":18,"description":"StudyTeam for Sites is a user-friendly clinical trial management system designed for clinical research sites. Sites can achieve recruitment and enrollment goals up to six weeks early by managing patient enrollment workflows in StudyTeam. StudyTeam’s mission is simple: accelerate clinical trial timelines. StudyTeam is both affordable and scalable, catering to each site's unique needs while enabling secure data-sharing with sponsors. Automatically de-identified data is shared with sponsors in real time, minimizing manual updates and reducing site burden. As a comprehensive solution, add the eSource suite for accurate source data capture and the Site Financials suite for efficient invoice and budget management.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/4b83ccd7-d981-4b93-8013-0103ca9c1439.png","url":"https://www.softwareadvice.com.au/software/250592/studyteam","@type":"ListItem"},{"name":"Nuvertos","position":19,"description":"NuvertOS is a healthcare management solution that helps hospitals, clinics, and more with managing health records, billing, pharmacy, diagnostic, and more. Specialized processes that are part of the offering allow the system to be configured and customized to the demands of the user.\n\nNuvertOS quickly made this action a reality, moving from one hospital to the next, clinic to clinic, and city to city. \n\nHow NuvertOS Safeguards Your Data ? \n\nTo make sure that your data is secure, NuvertOS goes above and beyond the standards set by the industry.\nThey adhere to recognized security patterns for encryption, hardening, authentication, and authorization. Their security team periodically reviews and improves our security posture. Additionally, data can be shared in the format needed with third parties or other systems without sacrificing security or privacy.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a1b64138-9dbd-4ca7-8a40-92816aa6eaa7.png","url":"https://www.softwareadvice.com.au/software/383718/nuvertos","@type":"ListItem"},{"name":"DFdiscover","position":20,"description":"DFdiscover is a cloud-based electronic data capture solution that allows healthcare organizations to streamline clinical trials by easily managing their study and trial phase needs as well as the data collection processes. It brings together data from diverse sources such as EDC, paper files and attachments in different formats and makes it easy for healthcare professionals to collect information from any source.\n\nWith DFdiscover, medical professionals can create reports, dashboards and workflows that reflect their own unique needs. The platform helps them to control data access with fine-tunable user roles, improve data quality and reduce queries by performing edit checks on incoming information. It also accelerates SDV and RBM processes by applying optical recognition that shaves time off manual data entry.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/be576228-d797-4921-9cc9-e2eb2bbc8adb.jpeg","url":"https://www.softwareadvice.com.au/software/265272/dfdiscover","@type":"ListItem"},{"name":"WeGuide","position":21,"description":"WeGuide is a web-based digital health platform that simplifies clinical trials and research studies by providing eScreening, eConsent, ePRO, eCOA and wearable data collection capabilities in a unified platform. It enables researchers and healthcare teams to launch patient engagement programs with form creation, multi-language support and seamless integration with existing health systems.\n\nThe tool optimizes patient experience and data quality. It provides tools for education, reminders and real-time monitoring. It supports diverse research and healthcare needs, from randomized controlled trials to telehealth and patient registries.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/a368c217-ca55-4fdd-b6aa-ed779c2ed904.jpeg","url":"https://www.softwareadvice.com.au/software/519063/WeGuide","@type":"ListItem"},{"name":"Ennov CTMS","position":22,"description":"Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, make better decisions, ensure compliance, select investigators well, manage finances, monitor patient recruitment. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers).  \n\nThis platform offers functions for tracking patients, patient visits, EDC data, queries, adverse events, deviations, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/9110455d-c6cc-49a4-b85c-1b4dbbd63373.png","url":"https://www.softwareadvice.com.au/software/311880/ennov-ctms","@type":"ListItem"},{"name":"Encapsia","position":23,"description":"Encapsia is a clinical data suite designed to help organizations streamline capturing, management, and reporting of electronic data in clinical trials. It includes an eSource app, which allows users to gather, validate, and clean data in real-time using iPad.\n\n\nThe Encapsia suite enables professionals to view data queries, tags, signatures, media attachments, and more. Features include historical records, audit trail, role-based permissions, navigation, gamification, data entry management, and offline access. Additionally, the multimedia functionality, allows users to record a variety of information including procedure videos, source notes, EMR screens, and informed consent.\n\n\nEncapsia’s loader and review apps let administrators define automated transfer rules for upload and review of third-party data. Further, enterprises can gain insight into trends, outliers, coded data and site performance via an analytics dashboard. 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/058803b6-7689-4eab-8f2d-e61d4d366b9d.png","url":"https://www.softwareadvice.com.au/software/105252/encapsia","@type":"ListItem"},{"name":"iMednet","position":24,"description":"iMednet is a cloud-based electronic data capture platform designed to help the healthcare industry capture, clean, adjudicate and manage data across clinical trials. The application enables research teams to build and implement study designs, prioritize tasks for trial execution and capture live data to generate reports in real-time.\n\n\nIt includes an ePRO module, which lets patients and research coordinators utilize a sign-on portal to enter study-specific information, create to-do lists and collect onsite or offsite data in compliance with regulations. iMednet also provides a data management tool with capabilities including randomization, inventory management, automated CEC adjudication and medical coding.\n\n\niMednet CTMS module enables clinical research teams to track various components of trials such as site payments, document collection status, potential risk assessments, transaction history, training reports and more on a unified platform. Pricing is available on monthly subscriptions.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/ad1c9f56-65de-4f7d-a384-26644f42fa05.png","url":"https://www.softwareadvice.com.au/software/138547/imednet","@type":"ListItem"},{"name":"Complion","position":25,"description":"Designed for hospitals, medical centers, trial sites and more, Complion is a cloud-based clinical trial management solution that helps handle manual processes on a centralized interface. The software automates investigator regulatory compliance, accelerating study startup and on-demand monitoring. With eRegulatory and eISF solutions, Complion helps users eliminate paper redundancies and site monitoring burdens. Additionally, Complion also provides real-time access to data for remote monitoring and decentralized trials, ensuring inspection readiness. It offers customer support via phone and email.","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductLogo/31e571ab-9d07-4099-9a2f-3df288fcf192.jpeg","url":"https://www.softwareadvice.com.au/software/301547/complion","@type":"ListItem"}],"numberOfItems":25}
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