Our state-of-the-art facilities follow GMP practices & global regulatory standards. Rigorous process validation ensures reliable, consistent scale-up.
Bringing a medical device from concept to global commercialization requires navigating complex engineering, regulatory, and manufacturing challenges. When these functions operate in silos, innovation slows and risks increase.
Syrma Johari MedTech partners with global MedTech innovators to design, engineer, manufacture, and scale regulated medical devices. Our integrated capabilities across development, manufacturing, and regulatory compliance help accelerate market entry while reducing program risk.
Prevent technology obsolescence with architectures designed for scalability, upgradability, and lifecycle continuity—ensuring your product stays relevant as markets evolve.
Integrated quality systems, global regulatory alignment, and validated processes ensure consistent performance and audit readiness across development and manufacturing.
Design-to-value, manufacturing efficiency, and managed services models reduce total cost of ownership while ensuring long-term product sustainability.
We build on decades of experience to provide customized solutions across every stage of the product lifecycle. Wherever you are in the journey, we are committed to driving your vision forward, helping you create differentiated and clinically meaningful products that succeed in the market.
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.
With 16 manufacturing sites, 4 design centers, and extensive global presence in India, Europe, and the U.S., Syrma Johari MedTech supports end-to-end medical device programs – from engineering to scalable, regulatory-compliant manufacturing.
Dedicated MedTech focus with deep domain expertise in key device segments.
Partnership at any stage of the product journey, or for full lifecycle ownership.
Integrated QARA support covering strategy, compliance, submissions, and audits.
Strategic presence in India, US & EU with resilient global supply chains.
End-to-end support to enable product development & market continuity.
Recognized for excellence in driving impactful MedTech innovations.
Recognized for excellence in driving impactful MedTech innovations.
Honored with “MedTech CDMO of the Year – Diagnostics and IVD” at the National Diagnostics Forum & Awards 2026.
Recognized as “Service Provider of the Year – Medical Supplies” at the ET Healthcare Awards for driving MedTech innovation through design-led manufacturing.
Honored with the National Export Excellence Award 2024 (ESC) for outstanding export performance in medical device electronics.
ET MSME Awards: Celebrating our excellence in MedTech manufacturing, innovation, and industry impact.
Design optimization, manufacturing scale-up, and regulatory integration enabling a compact, high-accuracy diagnostic platform for global point-of-care deployment.
Precision manufacturing, regulatory enablement, and component localization delivering cost-efficient, audit-ready production of endoscopic device.
Engineering-led redesign and manufacturing optimization delivering faster lysis, consistent sample processing, and scalable, cost-efficient production for global laboratory workflows.
Stay informed on regulatory developments, engineering best practices, manufacturing scale-up strategies, and industry trends in global MedTech markets.
Whether you’re an early-stage innovator or a global MedTech leader, SJML provides expert solutions tailored to your vision to expedite product realization and sustain your business growth. From first prototypes to high-volume global programs, we bring the structure, speed, and accountability needed to turn innovation into sustained market success.
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