Best Clinical Trial Management Systems - Page 15

Trialytix

Trialytix is the first software solution that covers all essential budget and cost operations of your clinical trial project.

UnitusTI

With UnitusTI's robust set of tools, your personal stamp is never lost, just streamlined.

Unlearn.AI

Unlearn.AI is at the forefront of integrating artificial intelligence into clinical research by developing AI-powered digital twins of patients. These digital replicas simulate individual health trajectories, enabling healthcare professionals to predict patient outcomes and compare potential treatment effects. By leveraging this technology, Unlearn.AI aims to eliminate trial and error in medicine, transforming clinical trials into more efficient, patient-centric processes.

Average Rating: 4.3/5.0

Total Reviews: 2

Veeva CTMS

With a real-time view across clinical trial processes, Vault CTMS improves operational efficiency, streamlines collaboration, and enables faster, higher-quality trial execution.

Veeva Vault Clinical Operations Suite

Velos eResearch

WCG Velos is a Clinical Research Management Solution (CRMS) designed to automate and centralize financial, operational, and administrative research activities. Leading research institutions, sites, and networks use the system’s integrated technology to consolidate and scale their research program, increasing profit, and improving protocol and regulatory compliance

WeGuide

WeGuide helps research teams, hospitals, pharma sponsors and CROs run studies and care programs on participants' own phones. One platform covers participant screening, eConsent with version control, re-consent tracking and audit trail, ePRO and PROM surveys, reminders and messaging, wearable data, patient registries and analytics. Wearable data comes from a native Garmin integration (including raw accelerometer and gyroscope data on supported models) and from Apple Health and Health Connect, which cover devices such as Apple Watch, Fitbit, Oura and Withings. Studies are BYOD first, and provisioned devices are supported when a protocol needs them. Data flows to REDCap through the REDCap API, and WeGuide also connects to Castor and Medidata Rave. WeGuide is Class I medical device software on the Australian Register of Therapeutic Goods (ARTG 355337), is ISO 27001 certified, and supports 21 CFR Part 11, HIPAA and GDPR requirements. In the BRACE trial led by Murdoch Children's Research Institute (6,800+ healthcare workers in five countries), participants logged daily symptoms in the WeGuide app.

Xolomon

XpertTrial

Your Research CTMS

Your Research is a leading Clinical Trial Management Software development company whose mission is to make a positive impact on people’s lives by advancing research processes that improve health outcomes. Your Research achieves this by offering the research industry a full suite of flexible, scalable, and integrable online modules derived from researcher led feedback. Your Research Clinical Trial Management System (CTMS) is tailored to streamline trials, prioritising patient-centricity and process efficiency. Key features include protocol-driven automation for time-saving and accurate data input. Patient experiences are enhanced through digitalisation, optimising in-person tasks, visit bookings, and eConsent with a focus on improving retention. Predict future events by tracking historical metrics. Access user-friendly 'pay per play' eCOA modules, such as ePRO, eConsent, and eCRF, to elevate trial efficiency. Your Research CTMS is a comprehensive integrable solution, ensuring a seamless and patient-focused research experience and is compliant with and or adheres to the following best practices: - HIPAA - 21 CFR Part 11 - Good Clinical Practice (GCP) - ISO 27001 - GDPR - FDA 21 CFR Part 50 - FDA 21 CFR Part 54 - ICH E6 (R2

Yuktii Clinov

Yuktii Clinov is medical practice management software combining appointment scheduling, patient records, clinical documentation, prescriptions, billing, and follow-up tools. Supporting 39 specialties, it offers workflows and templates for dental, primary care, specialty medicine, rehabilitation, and traditional practices. Patients can book appointments online with automatic updates. Reception features include queue management, check-in tracking, and no-show monitoring. Patient records consolidate medical history, visit notes, and communication logs. Clinical documentation uses specialty-specific templates, while the prescription module offers reusable templates, integrated drug lists, and PDF delivery via WhatsApp. Inventory management tracks stock, suppliers, and purchases. The billing system generates GST-compliant invoices and tracks balances. Follow-up tools include recall lists, reminders, and campaign messaging. Security features role-based access.

Zelthy-Clinical Trial Transparency

What is this product? Zelthy Clinical Trial Transparency is an application for pharmaceutical regulatory and compliance teams managing clinical trial disclosure obligations. It tracks submission deadlines across registries (ClinicalTrials.gov, EU CTR, and others), manages the preparation and filing of registry submissions and results postings, and performs cross-registry consistency checks to ensure disclosures align across platforms. Key Features & Functionalities - Deadline tracking across multiple clinical trial registries - Submission preparation and filing workflows - Results posting management with milestone tracking - Cross-registry consistency checks - Compliance calendar with automated reminders Primary Solution & Value Clinical trial transparency requirements have expanded significantly — FDAAA, EU CTR, and other regulations mandate timely registration and results posting with specific deadlines. Missed deadlines result in regulatory citations and reputational damage. This application tracks disclosure obligations across registries and automates deadline management, ensuring trials meet transparency requirements on schedule.

Zelthy-Compassionate Access

What is this product? Zelthy Compassionate Access is an application for pharmaceutical companies managing expanded access (compassionate use) programs. It handles the complete program workflow: patient request intake, physician and medical review, ethics committee approval, regulatory filing (FDA, TGA, EMA), and logistics coordination for drug supply — replacing the manual, multi-step approval process that often delays patient access to investigational therapies. Key Features & Functionalities - Patient request intake with physician documentation - Medical review and clinical assessment workflows - Ethics committee approval management - Regulatory filing for FDA, TGA, EMA, and other authorities - Drug supply logistics coordination - Program analytics and reporting Primary Solution & Value Expanded access programs involve a complex multi-step approval chain — medical review, ethics approval, regulatory filing — that can delay patient access to investigational therapies by weeks. This application digitizes the full approval workflow, reducing cycle time while maintaining the documentation required for regulatory compliance.