A Full-Service Independent Global CRO

Veeda Clinical Research Pvt. Ltd. derives its name from the Sanskrit word ‘Veda’, meaning knowledge or wisdom.

We are one of the largest Independent CROs in India with a scientific edge, better foresight for Early to Late phase clinical trials & an objective of becoming a catalyst for enhanced drug developments to facilitate better patient treatments.

With our 16 years of vast experience, we are serving our global clientele predominantly across Asia, Europe, USA & India. Our team at Veeda has more than 700 dedicated professionals to deliver Quality Clinical Research solutions coupled with robust scientific expertise & excellent regulatory knowledge to help pharmaceutical companies deliver life-changing therapies.

A Reliable Clinical Research Partner to the Pharma Fraternity

The success of a clinical trial is driven by the strategic selection of a reliable CRO. Our vastly experienced team of highly qualified professionals, a comprehensive portfolio of clinical research services to support diverse requirements and a robust Quality Management System guided and nurtured by our quality culture makes us a partner of choice for some of the leading pharmaceutical companies in the world.

Advancing Human Life with Scientific Excellence & Constant Innovation

Medical science is on a constant quest to develop better and more effective treatments, prevent diseases and provide accurate cure to human life. We aim at being a catalyst in this quest of advancing medical science forward.

We strongly believe in scientific excellence through teamwork and this has helped us rise to become one of the most competent partner for the (Bio) pharmaceutical companies across the globe.

Veeda constantly strives to be a partner for the pharmaceutical world by bridging the gap of bringing a therapy from Lab to Shelf and thereby contributing towards achieving the human ambition of having a longer, healthier and happier life.

Our Broad Range of Specialized Services

Bioavailability & Bioequivalence (BA/BE)

Helping pharmaceutical companies accelerate their regulatory submission and drug approval applications with our regulated bioequivalence and bioavailability studies.

Bio Analytical

Offering a full range of Bio Analytical Services supporting various aspects of the drug discovery and development to understand and estimate the complexity involved during execution.

Early Phase Clinical Development

Managing early phase clinical trials safely and efficiently in healthy volunteers & patients.

Late Phase Clinical Development

Offering comprehensive services for Phase II-IV clinical trials along with feasibility studies, regulatory submissions, site management, data management and more.

Bio-Pharmaceutics & Data Science

Delivering robust analysis and reports to ensure that projects stay on track, on time, and within budget.

Biologics & Biosimilars

Developing your biological drug in the clinical environment which is mandated for its acceptance in the major markets of the world.

Post Marketing Surveillance

Offering broad spectrum of high quality, flexible, cost effective and scalable safety monitoring services that can fit seamlessly into your process.

What Makes Veeda Special?

Patient Safety at the Core of Our Trials

The clinical research industry has come a long way from viewing patients as mere “subjects” to playing an integral part in the success of clinical trials. Subject and Patient safety is of utmost importance for Veeda and we take all measure in terms of infrastructure and resources to ensure the same.

Life at Veeda

The most valuable asset of an organisation is its human talent, and at Veeda we cherish our culture of diversity and inclusion. Our aim is to create an unparalleled Employee Value Proposition through innovative Learning and Recognition initiatives that puts our employees at the center of everything we do.

Entrusted by Regulatory Authorities

What our Clients say about us?