Welcome to Clinvia

Transforming Clinical Trials with Innovation and Automation

Clinvia is a next-generation, technology-driven CRO revolutionizing how clinical trials are designed, managed, and accelerated. We reduce costs and timelines by delivering AI-powered analytics, open-source driven and seamless digital solutions with regulatory compliance.

Partner with the Industry’s Leading Data Science Team

Clinvia LLC is a U.S.-based data science and technology company serving pharmaceutical and biotech clients worldwide. We partner with small to mid-size biotech innovators to streamline clinical development—from trial design to regulatory submission. Our flexible, high-touch model ensures speed, accuracy, and regulatory compliance at every step.

Unlocking Insights, Driving Innovation

Sudhir Singh

Managing Member and Principal Consultant

Our Services

At Clinvia, we provide end-to-end services that empower faster decision-making, improve data quality, and simplify operations. We help our partners bring therapies to market with confidence and agility.

Clinvia handles clinical studies of all sizes from Phase I-IV as part of our Function Services Provider (FSP) offering or as a standalone project. Whether you need Pharmaceuticals/Biotech/Medical Devices data management support, our dedicated clinical data manager is on the job. Clinvia consultants support Medidata RAVE, VEEVA, CLARIO, MEDDRIO and other EDC systems.


Our statisticians and programmers deliver robust analytics and submission-ready deliverables. From SAP development and interim analyses to SDTM/ADaM conversion and TFL generation, we support every phase with accuracy and regulatory expertise.

We bring the power of AI, machine learning, and big data to clinical research. Whether it’s predictive modeling, safety signal detection, or real-world data analytics, we craft scalable, cloud-based solutions tailored for speed and insight.

Why Clinvia​?

Trusted by Innovators for Speed, Precision, and Quality

Expertise that Delivers

Deep experience across biometrics, clinical operations, regulatory strategy, AI/ML, opensource and regulatory compliant technologies.

Real-Time, Actionable Insights

We convert raw clinical data into on-demand insights using advanced analytics and machine learning

Tailored and Agile Approach

Flexible service models designed to meet your unique needs—no matter the complexity of your study.

Quality from Start to Submission

Industry best practices, validated systems, and regulatory-grade outputs ensure audit readiness at every stage.

At Clinvia, we don’t just manage data—we unlock its power to accelerate cures and transform clinical trials.

Clinvia solves the challenges of slow, fragmented, and costly clinical trials by creating workflow automation, delivering real-time analytics, better data quality checks, integrated data science solutions, and AI-powered insights. From data management to regulatory submission, we streamline processes and empower decision-making, enabling biotech and pharmaceutical companies to bring life-changing treatments to patients faster and more efficiently.

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