ISO 13485 Medical Device Design Consultancy
What we offer:
Shore provides all our customers with a bespoke medical device development service under our fully accredited ISO 13485 development process.
Our team consists of experts in human factors, user interface, mechanical design, plastic moulding, complex mechanisms, material selection, fluid dynamics, finite element analysis, prototype manufacture, manufacturing set up and full production support.
Our in-house expertise includes development of orthopaedic devices, consumer medical devices, drug delivery systems, point of care products, trauma devices, implantable devices and cardiac diagnostics.
Our involvement covers all stages ranging from research and scenario definition, proof of concept, through engineering development and prototyping, tooling, into clinical trials and manufacture.
What are we looking for:
Should you have a desire to discuss your product, whether you are at the start of your development program or if you require assistance to solve a technical roadblock, we would be very keen to discuss options on how we could collaborate.
- Research & Development
- Technical Co-operation
- Commercial Agreement