Neucin Design has several year’s experience in the design, development and design history file management of medical devices in both class 2 and class 3 environments. Resulting in a thorough understanding and application of the regulatory, human factors and quality requirements as part of our development process.
This understanding combined with our staged design and development process allows us to manage these requirements effectively whilst adopting an agile and expedient approach enabling us to work flexibly within our client’s system to add value and meet their needs.
We consider the design for manufacture requirements early in the design process and integrate these throughout the development allowing us to advice and support manufacturing strategy, manufacturer selection and evaluation and commercial scale up.
Our adaptable approach combined with our dedicated, communicative and collaborative philosophy allows Neucin Design to deliver in meeting the needs and expectations of our clients.