An end-to-end, cloud-based platform for Clinical Trials with fully modular tools that allow you to pick and configure them according to your needs.
Transform your business with Joule, agents, and SyMetric's AI operating system, November 4-6, 2025.
Our Philosophy
Our platform is built for the cloud era with modular, integrated tools that are designed to provide flexibility. Whether you are a Pharmaceutical Company, Clinical Research Organization, or an Academic Institution, our Platform can be tailored to your Study requirements, including Adaptive Trials, Umbrella Trials, Basket Studies, and Virtual Clinical Trials.
Get StartedA comprehensive, modular suite to power every aspect of your clinical trial.
Role-Based Access Control and Self-Service Account Management.

Clinical Trials are conducted by numerous organizations which employ several highly skilled teams and individuals to perform unique and complex roles. For a Trial to be successful, the activities and tasks of these Teams and Individuals must be synchronized and documented.
The SyMetric Platform provides a virtual collaborative environment that is secure, user-friendly, and intuitive.
It streamlines the communication among the multiple teams involved in a Trial and provides the necessary tools for effective data capture and decision-making. This Collaboration Model along with fully customizable role-based authorizations enables teams and individuals with secure and real-time access to Trial Data.
Over the years, we have delivered safe and reliable solutions to all our clients across India and abroad.
We prove our commitment to our Global Customer base by ensuring regulatory compliance and security.
Our Clinical Trial Platform is a SaaS Solution that is available with the most trusted and compliant Cloud-Hosting options.

Contact us for customized Cloud Solutions
Get in touch with us to customize your solutions — whether for a dedicated single-tenant solution or a completely custom deployment model.
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A modularized experience that allows seamless integration and scalability for your trials.
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An easy-to-use interface that reduces training time and increases user adoption.
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Access all platform tools with a single, secure login, simplifying user management.
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Highly adaptable to your specific research study protocols and unique workflows.
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Save time and ensure consistency by creating and reusing forms and business rules across studies.
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Adheres to 21 CFR Part 11 and ICH-GCP guidelines, ensuring data integrity and audit readiness.
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Gain instant visibility into trial progress with powerful real-time dashboards and analytics.
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Integrate with wearables, medical devices, and external AI systems for image analysis using modern standards like DICOM.
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Our expert technical support team is always available to ensure your trials run smoothly.
Explore MoreOur system design ensures full compliance with federal regulations like **21 CFR Part 11**, with a proven track record for maintaining data integrity, security, and electronic signatures as per FDA regulations. Data security is an implicit part of our product development, with security features built from the ground up, backed by our team of experts.
We ensure you meet regulatory requirements like **GDPR** and **HIPAA** through proactive measures. Our strict data governance policies ensure the use and disclosure of PHI is well-governed, and the collection, storage, and use of personal data is always justified and consent-based.
Read our privacy policySystem processes are designed around **ICH-GCP** and **GMP** guidelines to ensure subject safety and product quality. Our solution is also fully compliant with **GS1** requirements, providing a common framework for identifying, capturing, and sharing data across all stakeholders.