End-to-End Technical Consultancy for Medical Device Development, Injection Mould Engineering, Scientific Injection Moulding, Qualification & Validation, Manufacturing Engineering, and ISO 13485 Compliance.
Helping medical device companies transform ideas into commercially successful, high-quality, and regulatory-compliant products.
NexOra MedTech provides specialized technical consultancy in Medical Device Development, Injection Mould Engineering, Scientific Injection Moulding, Qualification & Validation, Manufacturing Engineering, and ISO 13485 & U.S. FDA 21CFR Part 820 requirements.
We are currently building a comprehensive website that reflects the depth of our engineering expertise and technical capabilities.
While our digital platform is under development, NexOra MedTech is fully operational and ready to support medical device companies with engineering consultancy, manufacturing excellence, qualification & validation, and regulatory compliance.
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SAME COMMITMENT.
A BIGGER VISION AHEAD.
NexOra MedTech is a technical consultancy dedicated to supporting medical device companies throughout the product development lifecycle. We work closely with startups, established manufacturers, pharmaceutical companies, and OEMs to transform innovative ideas into robust, manufacturable, and regulatory-compliant products.
With more than 13 years of practical engineering experience, our focus is on delivering technically sound, efficient, and scalable solutions that reduce development risks while improving product quality and manufacturing performance.
From product development and precision tooling to scientific process development, validation and manufacturing support, NexOra MedTech provides practical engineering expertise for medical device and precision plastic component projects.
Conversion to engineering design, DFM, prototyping and design support for medical devices and drug-device combination products
High-precision mould design review, development, technical assessment, optimization and manufacturing support
Scientific process development, rheology, cavity balance, DOE, process optimization and robust manufacturing process establishment
IQ, OQ, PQ, mould qualification, process validation, capability studies and engineering validation for controlled manufacturing processes
Process development, technology transfer, mould-machine mapping, production scale-up, capacity planning and manufacturig support
Quality management systems support, engineering & validation documentation and technical readiness for regulated medical-device manufacturing
With 13+ years of hands-on experience in plastics engineering, medical device manufacturing, injection mould development and scientific injection moulding, NexOra MedTech brings practical engineering expertise to medical-device projects.
13+ Years of Engineering Experience – Practical engineering and manufacturing expertise
Scientific Engineering Approach – Data-driven process development, DOE and troubleshooting
Development to Production – From product and mould development through scale-up
Medical Device Industry Focus – Engineering support aligned with quality and regulatory requirements
Whether you're developing a new medical device, optimizing a manufacturing process, developing an injection mould, or working on qualification and validation, NexOra MedTech is ready to support your project.
📧 Email : ssavalia@nexora-medtech.com
📱 Contact us : +91 9726 5152 83
📍 Location : Rajkot, Gujarat, India