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India must build export-oriented medical devices industry, says pharma secretary

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India must build export-oriented medical devices industry, says pharma secretary

by Asia Today Team
August 8, 2026
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New Delhi: India should transfer past import substitution strategy within the medical gadgets sector and construct an export-oriented business that serves world markets, a senior authorities official stated on Friday.

For this, the nation must strengthen its home element manufacturing and deepen worth addition, Secretary, Division of Prescription drugs, Manoj Joshi, stated.

The medical gadgets sector must be considered from each healthcare and business perspective, he stated addressing the ‘India Medical System 2026’ occasion, organised by business physique FICCI within the capital.

“India should transfer past the import substitution strategy and construct an export-oriented business that serves world markets. Whereas the Indian medical gadgets market is valued at round USD 16 billion, the worldwide market exceeds USD 600 billion, providing immense alternatives for Indian producers,” he famous.

To understand this potential, Joshi stated,”It’s important to strengthen home element manufacturing, deepen worth addition, facilitate seamless cross-border motion of elements and merchandise, combine India into world worth chains, and foster stronger partnerships between startups and huge industries in order that improvements can efficiently attain the market.”

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Whereas healthcare suppliers concentrate on entry to high quality gadgets regardless of their origin, home manufacturing is important to generate employment, strengthen business capabilities, and guarantee provide chain resilience particularly throughout world disruptions, Joshi famous.

Talking on the occasion, Medicine Controller Normal of India (DCGI) Rajeev Singh Raghuvanshi stated India’s medical gadgets sector is present process a elementary transformation from an import-driven market to a home manufacturing-led ecosystem.

There’s a must strengthen indigenous capabilities in high-end medical gadgets and ‘in vitro’ diagnostics, whereas making certain sooner, clear and predictable regulatory approvals, he stated.



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