MEDICA 2025 Conference Düsseldorf | 17 – 20 Nov 2025
Driving End-to-End MedTech Solutions
From Design & Engineering to Global Manufacturing & Regulatory Compliance
See us at MEDICA & COMPAMED 2025
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Our Group Presence
Syrma SGS Technology Limited, together with Syrma Johari MedTech Ltd. and SGS Solutions GmbH joins the global MedTech community in Düsseldorf this November. Explore how we blend design-led innovation, engineering precision, and global manufacturing and regulatory excellence to deliver next-generation medical devices.
As a group, we’re excited to meet Global MedTech partners and collaborators at MEDICA & COMPAMED 2025 in Düsseldorf.
Engineering Innovation. Manufacturing Excellence. Enabling Compliance. Empowering Global MedTech.
Syrma Johari MedTech Ltd. (SJML) partners with leading OEMs worldwide to accelerate device innovation through advanced engineering, scalable manufacturing, and full regulatory compliance (FDA, ISO, CEE).
With strategic European operations at SGS Solutions GmbH in Stuttgart & Winnenden, we deliver engineering innovation, manufacturing excellence and end-to-end product realization for European partners.
MDSAP-Certified | FDA, ISO & CEE Compliant | Global Footprints in India, Europe & USA
Our Focus Areas

High-Precision Manufacturing Scale
Our cutting-edge solutions span a broad range of segments including diagnostics, imaging, physiotherapy and rehabilitation, medical aesthetics, patient monitoring, and connected health.

Fast-Track Development
Faster time-to-market through agile design and engineering.

DFM & System Integration
Optimizing every stage from concept to assembly.

Regulatory Readiness
Proven compliance with FDA, ISO 13485, CEE, and MDSAP frameworks.
Meet Our Experts at MEDICA & COMPAMED 2025
Managing Director, SGS Solutions GmbH
Leading European operations with a focus on strategic customer engagement and market development across DACH and EU regions.
Vice President – Sales, Syrma SGS Group
Driving global sales and partnerships with OEMs in Europe; specializing in MedTech manufacturing collaborations, customer-focused innovation and large-scale delivery programs.
Why Meet Us?
India’s first MDSAP-certified, design-led MedTech manufacturing partner
Robust Quality Management System (QMS) aligned with ISO 13485, EU MDR, FDA QSR, and other global regulatory frameworks
Global footprint across Germany, India, and the U.S., enabling cost-efficient, high-quality manufacturing and supply chain resilience.
End-to-end MedTech solutions spanning design, manufacturing, and regulatory affairs for accelerated go-to-market
Strategic regulatory guidance for rapid market entry and post-market support across U.S., Japan, the Middle East, and other major markets
Our Success Stories
Cost-Effective, Scalable Manufacturing for a Life-Saving IVD Platform
Client: Medical diagnostics firm developing point-of-care testing devices
Solution Delivered: Design for Manufacturability (DFM), value engineering, manufacturing, regulatory submissions
Impact: 45% faster development-to-manufacturing cycle, 20% cost savings
Scaling Medical Device PCB Assembly with Custom-Developed Automated Test Fixtures
Client: MedTech company specializing in Class II orthopedic therapy and rehabilitation systems
Solution Delivered: Supply chain management, PCB assembly, plasma coating of PCBAs, validation using cutom-developed test fixtures
Impact: ~3x higher test throughput (30 sec to 3 min per unit)
How Our Turnkey Regulatory Solution Accelerated Global Market Readiness for a Medical Aesthetics Leader
Client: Top-tier medical aesthetics OEM
Solution Delivered: Supplier assessment, DHF and DMR remediation, regulatory submissions, risk management, product complaints management
Impact: 125% improved supplier oversight and compliance coverage, 55% bandwidth savings for the client’s internal resources, 40% reduced operational cost
Streamlining Medical Device Global Regulatory Submissions for Faster Go-to-Market
Client: Ophthalmic device manufacturer specializing in diagnostic and imaging solutions
Solution Delivered: Regulatory strategy and global submissions support
Impact: 80+ international markets covered, 100% documentation submitted as per regional regulatory timelines
Let’s connect at MEDICA & COMPAMED 2025 in Düsseldorf!
Schedule an exclusive meet-up with our leadership team and explore how we can accelerate your next MedTech innovation.
