Custom-Built for Your Needs
Zelthy offers a fully customizable decentralized clinical trial management solution that adapts to any trial type, specialty, or workflow. Whether you're running small pilot studies or large-scale global trials, Zelthy ensures your processes are supported, not the other way around, providing flexibility and scalability that grows with your needs.
Patient-Centric Design Enhancing Engagement and Retention
Our platform puts patients first, simplifying their trial experience with features like virtual recruitment, eConsent, and mobile-enabled ePRO/eCOA submissions. This approach not only enhances the quality of data collected but also ensures a smoother trial experience for participants, regardless of their location.
Robust Data Management with Uncompromising Compliance and Security
Zelthy ensures the integrity and confidentiality of trial data with a secure platform that meets global standards like FDA, GDPR, HIPAA, and 21 CFR Part 11. With features such as encryption, audit trails, and e-signatures, our solution supports real-time data capture and analytics while maintaining strict compliance.
Globally Adopted
A global partner with extensive experience in more than 10 countries.
2M+
Patients
1000+
Applications
3000+
Hospitals
5000+
Doctors
Key Features
Patient Recruitment and Engagement
Our eRecruitment solutions, coupled with timely text reminders, interactive live chat and a comprehensive patient portal ensure robust engagement levels.
Electronic Consent (eConsent)
Zelthy simplifies the consent process with multimedia consent options, supported by built-in video conferencing technology, making it easier for participants to join from remote locations.
Integrated ePRO and eCOA Solutions
With Zelthy's native ePRO app, patients can easily submit data through multi-media enabled interfaces on their mobile devices, ensuring accurate and timely data collection.
EDC with Seamless Integration
Our platform easily integrates with existing systems to enhance data reliability and oversight, making it simpler to manage and monitor trial progress effectively.
Direct-to-Patient Capabilities
Manage investigational product shipments directly to patients with secure patient confirmation systems, enhancing convenience and compliance.
Seamless Integration with Mobile and Health Devices
Our platform supports seamless API integration for real-time biometric data collection from various mobile and health devices, enriching data with digital endpoints.
Remote Monitoring and Source Data verification
Zelthy enables efficient off-site monitoring and remote source review, ensuring compliance and integrity of trial data without the need for on-site visits.
Reporting and Analytics
Gain insights with real-time intelligence and interactive dashboards, allowing for detailed data visualization reports and effective performance tracking.
Budget and Payment Management
Zelthy aids in budget estimation and streamlines payments management, ensuring timely investigator grants and financial oversight.
Discover the essential components and latest advancements in Clinical Trial Management Systems (CTMS) for 2025 in this comprehensive guide. Learn how these systems streamline operations, enhance data management, and improve participant engagement in modern clinical trials.
FAQ
What are decentralized clinical trials (DCTs)?
Decentralized clinical trials (DCTs) use digital tools and remote technologies to conduct clinical research outside of traditional clinical settings, such as hospitals or clinics, allowing for greater patient convenience and access.
What are the main benefits of decentralized clinical trials?
DCTs offer increased patient accessibility, reduced trial costs, enhanced patient engagement, and faster recruitment by leveraging remote technologies, telemedicine, and digital data collection.
How do decentralized clinical trials improve patient recruitment?
By using virtual patient recruitment tools and online platforms, decentralized clinical trials can reach a larger, more diverse patient pool, making it easier to recruit participants from various geographical locations.
How is data collected in a decentralized clinical trial?
Data is collected remotely through mobile apps, wearables, ePRO, and eCOA tools, enabling real-time, accurate tracking of patient-reported outcomes and clinical assessments.
How does eConsent work in decentralized clinical trials?
eConsent allows patients to review, sign, and submit consent forms electronically using digital signatures and multimedia options, all through a secure platform, making the process more accessible and efficient.
What technologies are used in decentralized clinical trials?
DCTs leverage various technologies, including telemedicine, remote monitoring, mobile health apps, wearables, and electronic data capture (EDC) systems to streamline operations and enhance data collection.
Are decentralized clinical trials compliant with regulatory requirements?
Yes, decentralized clinical trials are designed to meet regulatory standards like FDA, HIPAA, and GDPR, ensuring that data is secure and that all trial processes are conducted in compliance with the law.
How does remote monitoring work in decentralized clinical trials?
Remote monitoring allows study teams to track patient progress, collect data, and verify source data without requiring patients to visit a physical site, ensuring continuous oversight and improving data integrity.
Can decentralized clinical trials improve patient retention?
Yes, by offering a more convenient and flexible experience, including virtual visits and easy access to trial information, decentralized trials can lead to higher patient retention and engagement.
What is the role of wearables in decentralized clinical trials?
Wearables and sensor integration play a critical role in capturing real-time biometric data from participants, enriching the trial with valuable insights and enabling continuous monitoring.
We recommend getting an opinion from an expert first.