Audience
Hospitals
About Folio3 Clinical Trial Management
Folio3 Digital Health's Clinical Trial Management Software (CTMS) is a comprehensive, web-based platform designed to streamline the entire clinical trial lifecycle for pharmaceutical companies, CROs, and research organizations. It centralizes trial operations, from planning and site management to data collection and reporting, ensuring compliance with global regulations like FDA 21 CFR Part 11, GxP, and HIPAA. The software emphasizes user-friendly interfaces, real-time dashboards, and scalable modules to handle trials of any size efficiently.
Core Modules
The platform features dedicated modules for study setup, where users define protocols, timelines, and budgets with customizable templates. Site management tools track investigator qualifications, contracts, and payments, while patient recruitment capabilities include screening, enrollment tracking, and visit scheduling with automated reminders.
Other Popular Alternatives & Related Software
Cloudbyz CTMS
Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc.
Cloudbyz 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.
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Longboat
Longboat is a cloud-based clinical trial support solution provides users with an integrated Guided Compliance toolset to guide them at all times. Longboat provides the clinical trial site staff with the right resources to let them focus on patients. Longboat allows patients to view essential study information and check visit reminders. Longboat allows users to seamlessly manage the controlled rollout of the amended clinical trial protocol. Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders. All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs. Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant.
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AQ Platform
AQ Platform is clinical research management software for NHS trusts, investigator sites, clinical trials units, site networks, CROs, sponsors and academic research teams. Its modules cover trial management, electronic trial and investigator site files, pharmacy and laboratory workflows, quality management, CAPA, and digital delegation of authority. Shared governed trial records and audit trails connect study operations. Connected Intelligence uses AI to flag gaps and draft next steps; a named user confirms each proposal, and customer data is not used to train models. Hosted in Microsoft Azure UK regions, the platform is designed around ICH E6(R3) and MHRA GCP inspection expectations. AQ Trials holds NHS DSPT Standards Met (2026) and Cyber Essentials certification. Phase 1 trial doctors built it; modules can be deployed individually, and it has been in daily NHS use since 2020.
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HEKMA
HEKMA is an AI-powered clinical trial intelligence company focused on accelerating clinical research by improving patient recruitment, trial feasibility, and patient engagement.
The company serves CROs, pharmaceutical sponsors, hospitals, and patients through an integrated platform that connects electronic health records (EHRs), AI-driven trial matching, clinical trial management, and patient engagement tools.
Its mission is to reduce enrollment delays, improve access to clinical trials; particularly for underserved populations and make clinical research more efficient, transparent, and patient-centric.
HEKMA combines expertise in healthcare, artificial intelligence, and clinical operations while maintaining compliance with industry standards such as HIPAA, 21 CFR Part 11, GDPR, and HL7/FHIR.
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Pricing
Starting Price:
$300
Integrations
No integrations listed.
Company Information
Folio3 Digital Health
Founded: 2005
United States
digitalhealth.folio3.com/solutions/clinical-trial-management-software/
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Product Details
Platforms Supported
Cloud
Windows
Mac
iPhone
iPad
Android
Chromebook
On-Premises
Training
Not Offered
Support
24/7 Live Support
Online
Folio3 Clinical Trial Management Frequently Asked Questions
Q: What kinds of users and organization types does Folio3 Clinical Trial Management work with?
Folio3 Clinical Trial Management works with these users and organization types: Mid Size Business, Small Business, Enterprise, Freelance, Nonprofit, Government, and Startup.
Q: What languages does Folio3 Clinical Trial Management support in their product?
Folio3 Clinical Trial Management supports these languages: English.
Q: What kind of support options does Folio3 Clinical Trial Management offer?
Folio3 Clinical Trial Management offers support via 24/7 live support and online.
Q: Does Folio3 Clinical Trial Management have a mobile app?
Yes, Folio3 Clinical Trial Management has a mobile app for iPhone, Android, and iPad.
Q: What type of training does Folio3 Clinical Trial Management provide?
Folio3 Clinical Trial Management provides training in the form of not offered.
Q: How much does Folio3 Clinical Trial Management cost?
Pricing for Folio3 Clinical Trial Management starts at $300.
