Make In India For The World

Driving Global MedTech Innovation

Look at India. Look at Endless Possibilities in Medical Device Manufacturing. India has evolved into a strategic global hub for MedTech innovation and manufacturing, making significant strides in manufacturing excellence and leadership. 

Partner with Syrma Johari MedTech to design, manufacture, and commercialize compliant medical devices for global markets. 

Make in India: From Vision to Value Delivered by SJML

Driving precision manufacturing, regulatory compliant quality, scalable capacity, faster time to market, and sustainable cost advantage for our MedTech Partners.

USA | Hematology Diagnostics

Design & Scaled Manufacturing of a Microchip Electrophoresis Point-of-Care IVD Platform

Design optimization, manufacturing scale-up, and regulatory integration enabling a compact, high-accuracy diagnostic platform for global point-of-care deployment.

EU | Minimally Invasive Devices

Localization & Scaled Manufacturing of Advanced Endoscopic Imaging Systems Under the Make in India Program

Precision manufacturing, regulatory enablement, and component localization delivering cost-efficient, audit-ready production of endoscopic device.

Why Global MedTech is being Designed & Manufactured in India?

India delivers world‑class medical device manufacturing through a unique convergence of scale, talent, policy support, and cost management.

Source: India Brand Equity Foundation

Vision: Leading the World Through Technology and Manufacturing Excellence

Source:  Invest India 

Key Government Initiatives

Make In India → Make For The World

Production Linked Incentive (PLI) Scheme for Domestic Manufacturing of Medical Devices – $ 455.2 Mn

FDI for Manufacturing under automatic route – 100%

Regulatory Streamlining – A Single Window Clearance System for Licensing of Medical Devices

Medical Device Parks – $10 Mn each

Syrma Johari MedTech Expertise

Syrma Johari MedTech is One-Stop-Solution for Medical Device Technologies throughout the Product Lifecycle – from concept to commercialization.

Design & Engineering

Manufacturing

Compliance Services (QARA)

Product Lifecycle Management

Concept-to-prototype medical device development, integrating system requirements and architecture with full-stack engineering, ensuring manufacturability.

ISO 13485–certified manufacturing, including precision manufacturing, global supply chain solutions, and medical plastics manufacturing.

Global submissions support, audit readiness, risk management, and post-market regulatory support.

Sustaining product viability and value post-launch through sustenance engineering, value analysis and value engineering (VAVE), and regulatory sustenance programs.

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