Your product works. Is it ready for the market?
We help MedTech companies close the gap between engineering and regulatory approval and bring that same rigour to broader technology and product development work.
What We Do
Pick the one that matches your requirement
Product Design & Development (NPI/NPD)
Concept to Production – product design, engineering, and new product introduction
Technology Consulting & Application Development
Cloud and mobile app development, embedded/IoT, and AI/ML solutions
MedTech Regulatory & Compliance
ISO 13485, IEC 62304, EU MDR and the full path to market
Working with startups and established organisations around the globe, spanning India, the US, Europe, and the Middle East.
How We Work
A simple four-step model, from first conversation to handover.
01
Connect
We start with a conversation about your product, stage, market and constraints. A short fixed-price assessment is available if you want a defined first step.
02
Synergise
We shape the plan and bring in the right specialists for each phase, with one senior point of accountability throughout.
03
Deliver
We design, build, document and test, managing accredited-lab testing where needed, with weekly progress reports.
04
Support
We hand over complete design documentation and stay available for sustaining engineering and regulatory support.
Who We Serve
Startups and founders
You have a product that works but limited budget or regulatory know-how. We scale engineering and quality to your stage, so compliance is built in from the start.
Mid-size organisations
You want to test or scale a product, prototype or software without building a full in-house team. We bring engineering and compliance together under one accountable lead.
Engagements of any size and length, billed hourly or monthly.
A Note from the Founder
With a career built at the intersection of engineering, technology and regulatory compliance, I have spent years helping organisations turn ambitious product ideas into safe, compliant, market-ready realities. My expertise spans the full lifecycle of regulated product development, from design controls and risk management to software, hardware, and systems engineering, guided by international standards including ISO 13485, ISO 14971, IEC 62304, and IEC 60601.
Having led cross-functional engineering teams through the rigorous path to regulatory submission readiness, brought legacy products into audit-ready compliance, and built the quality and technical documentation, I know what regulators and notified bodies expect.
GAURAV TECHNOLOGIES LLP was founded to bring that same depth of expertise and engineering leadership to startups and growing companies who need a trusted partner to navigate compliance, design, and delivery without the overhead of a large consultancy.
Let’s Talk
If you’re building a product and trying to figure out what compliance or market approval you require or keeping quality systems from becoming a bottleneck, we’d like to hear where you’re stuck.