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Life Sciences India 2025: Law and Practice
Chambers & Partners Global Practice Guide Offering Comparative Analysis
June 12, 2025
The life sciences sector in India is rapidly evolving, driven by advances in technology, shifting public health priorities, and increasing global integration. As one of the most heavily regulated industries, the pharmaceutical and medical devices ecosystem in India is governed by a combination of laws and compliance requirements. Understanding this regulatory landscape is crucial for businesses, regulators, healthcare professionals, and investors navigating the Indian market.
Drawing on its life sciences law experience, NDA contributes to the India chapter to the Chambers Life Sciences Guide 2025 to help stakeholders better understand the country’s complex regulatory framework.
The guide offers in-depth analysis of India’s legal and regulatory framework across the product lifecycle, from R&D and clinical trials to marketing, manufacturing, distribution, and pricing. It also covers data protection, post-marketing obligations, regulatory reliance mechanisms, and recent legislative developments. Designed as a practical reference, the chapter provides critical insights into licensing processes, fast-track pathways, public procurement, and market access challenges in India’s dynamic life sciences ecosystem.
Please click
here to access our paper.
Regards,
Uttara Jhaveri,
Tanya Kukade,
Eshika Phadke and
Dr. Milind Antani
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