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With ISO 13485 registration covering product development from first concept right through to short run manufacture, CDP will partner with you right up to manufacturing your first few batches for clinical or consumer trials.

By having a single team responsible for both user-centred design and manufacturability, a healthy tension is maintained throughout the development process and the all-too-frequent problems of transfer to manufacture - where these contrasting requirements too often meet for the first time - are avoided.

Scale-up to volume manufacture is planned in from the outset, with pilot lines mimicking the exact process that is envisaged for full automation with jigs and fixtures removing human variability for the critical process steps.

Our development of the manufacturing process as well as the product gives our clients ownership of any IP and knowhow arising and ensures freedom of choice regarding suppliers and CMOs.

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