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Our Success Stories
Explore how Syrma Johari MedTech is supporting global MedTech leaders in bringing breakthrough devices to market with unmatched expertise and cutting-edge technology.
Why Choose Syrma Johari MedTech
One-Stop MedTech Partner
Our integrated ecosystem offers end-to-end support across the product lifecycle, ensuring a seamless journey from concept to aftermarket.
Faster Go-to-Market
With scalable manufacturing infrastructure and global supply chain solutions, we accelerate market entry by 30–40%.
Innovation at the Core
By combining expansive domain expertise with cutting-edge technology, we drive groundbreaking innovation across diagnostics, therapeutics, medical aesthetics, and more.
Our Global Presence
Jodhpur, India
Pune, India
Design & Innovation
Business Development
402, Tower 2, World Trade Center, Kharadi, Pune – 411014, India.
Europe
USA
Let’s Accelerate Your Next MedTech Innovation!
Frequently Asked Questions
Which regulatory standards does Syrma Johari MedTech comply with?
Syrma Johari MedTech operates ISO 13485 and US FDA–certified facilities, following Good Manufacturing Practices (GMP) across all manufacturing operations. Our Quality Management System (QMS) is structured in accordance with ISO 13485, MDSAP, FDA Quality System Regulation (21 CFR Part 820), EU MDR, UKMHRA, Japan’s MHLW, Health Canada, and India’s CDSCO, along with other applicable international regulations. This integrated compliance framework ensures consistent product quality and reliability across every market we serve.
Which quality control processes do you have for manufacturing medical devices?
Our quality control framework includes rigorous supplier assessment and qualification, raw material quality inspection, in-line inspections during production, and final product validation. Continuous improvement is driven through KAIZEN initiatives, Corrective and Preventive Actions (CAPA), Engineering Change Requests, and statistical reviews. We maintain Device History Record (DHR) for end-to-end traceability across production batches.
Are your devices customizable for specific design requirements?
Yes. We offer complete customization of devices to meet specific design requirements. Our design and engineering teams collaborate closely with clients during the development phase to ensure every technical specification is met. Prototype validation is conducted before mass production to ensure optimal performance and alignment with customer expectations.
What is your capacity for scaling production?
We operate 14 global manufacturing facilities with scalable infrastructure and a diversified supplier network. Our 34 high-speed SMT lines support an annual PCB assembly capacity of over 5 million units. This robust setup enables seamless scale-up from prototype to high-volume production while maintaining consistent quality and stringent regulatory compliance.
How do you incorporate the latest technological advancements into your solutions?
We adopt a structured approach to ensure our products and processes remain at the forefront of technology. Sustenance engineering is performed through continuous post-market surveillance and feedback-based product enhancements. Our dedicated R&D team monitors emerging trends and collaborates with strategic partners to drive innovation.
Manufacturing processes are updated in real time as designs evolve, ensuring alignment with the latest technologies. We also place strong emphasis on ergonomic, user-centric device design to meet evolving customer and market needs.