India as a Destination for Clinical Trials

For sponsors in the United States and European Union, India offers a rare combination of scale, speed, and cost efficiency without compromising data quality. The country is home to roughly 18% of the world’s population, yet only a small share of global clinical trials are conducted there, providing access to a large, undertapped, and often treatment-naïve patient base.

Read our white paper that learn about how Independent analyses report trial costs in India run materially below Western markets, recruitment that is faster than global averages, and how to achieve a regulatory framework with statutory, predictable approval timelines. This paper lays out the evidence-based case for including India in multiregional clinical trial (MRCT) programs.

Why India Is a Strategic Advantage for Clinical Trials

Discover how India’s scale, cost efficiency, faster patient recruitment, and predictable regulatory timelines can strengthen your multiregional clinical trial strategy.

Download the White Paper

Explore the evidence behind India’s advantages in clinical research, including faster patient recruitment, cost-efficient trial execution, access to a large treatment-naïve population, and predictable regulatory timelines. This white paper outlines the strategic case for including India in multiregional clinical trial (MRCT) programs