SyMetric Clinical
Trial Platform

Designed and built to be an end-to-end platform for Clinical Trials, this Cloud-Based Solution features fully modular tools that allow you to pick and configure them according to your needs.

Built With
Purpose

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.

Overview of Tools on Our Platform

Explore Our Solutions

IRT/IWRS

Developed with years of strong industry expertise and tested to deliver against the most complex Clinical Trial designs, our IRT/IWRS solution is the most comprehensive one in the market today.

EDC

The Electronic Data Capture solution includes well-designed tools that transform the Data Management processes and simplify and automate the Data flow and validation of Data in Clinical Trials.

CTM

The Clinical Trial Master provides various repositories to maintain Global objects, including a repository of Trial Sites, Labs, Organizations, Global Data Libraries, and more.

Our Collaboration Vision

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.

CTMS

Affordable and Scalable, Globally

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.
SyMetric
EDC
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Looking for Customized Hosting
and Deployment Models?

Our Clinical Trial Platform is a SaaS Solution that is available with the most trusted and compliant Cloud-Hosting options.
Microsoft
SAP
Clouds
Get in touch with us to customize your solutions — whether for a dedicated single-tenant solution or a completely custom deployment model.

The SyMetric Advantage

Increase trial efficiency and reduce costs with multicomponent (IWRS/IRT, CTM, and EDC) solutions built up as a single integrated solution.

A user-friendly layout complemented with a simple look and feel of the application assures enhanced user experience and increased control of the interface.

The integrated cloud-based platform allows a Single Sign-On feature to streamline the user authentication process. The user can sign on to access all the authorized tools with a single set of credentials, avoiding cumbersome multiple sign-ins.

Tailored application design to suit all types of research study patterns with minimal configuration changes.

Import unique CRFs with standardized data definitions and associated business rules from the Global CRF Library to eliminate form re-designing efforts.

Our FDA 21 Part 11- and ICH-GCP-compliant application is featured with procedural controls, audit trails, and electronic signatures to safeguard the confidentiality and integrity of data.

Visually track and analyze key performance indicators and site metrics for the study with customized reports and dynamic dashboard information.

Expert technical team rigorously trained on the Application provides round-the-clock support for quick issue resolutions with minimal turnaround time.

Security and Compliance

Security and Compliance
Build data security from the ground up with the backing of our team of experts. We ensure that you meet regulatory requirements (Data protection laws, Good Clinical Practice guidelines, and more) through proactive compliance measures that use well-defined policies, processes, and a robust Standard Operating Procedure framework. Our methods are trusted by large Pharmaceutical Organizations, CROs, and Academic Institutions.
ISO 27001
ISO 9001
21 CFR Part 11 (US FDA)
ICH-GCP

Uncompromised Commitment to Data Privacy

We go to great lengths to ensure that you have full control over data that powers your research. When it comes to data privacy, our resolve is unmatched and we are only custodians of data that is yours.
Data Privacy