David Warwick
David Warwick, Director, eg technology Ltd
With extensive experience in the MedTech and BioTech sectors, David joined eg in 2008 and was appointed as a Director in 2019. As part of his role, he provides overall project monitoring, reporting, delivery and strategic direction. He is a senior point of contact for clients and the technical lead for multiple projects, using his experience to identify and address issues and to set the overall technical direction. His expertise is invaluable in providing insight into various regulatory aspects of medical devices, whether that's designing for compliance and the application of standards or specifications and testing. As a director, he has an overall responsibility for bringing in new business and works with the senior management team to consistently evaluate business operations to ensure strategic growth.
Turning research into successful medical devices: understanding the development process & accelerating your route to market.
The design and development of medical devices can be a complex process and defining the initial steps is just the start. Our extensive experience enables us to share an overview of the spectrum of challenges and risks associated with the design and development of medical devices, from the inception of the development programme to identifying user and product requirements and how to leverage different prototyping techniques to de-risk the development and make a better product.
• We will share the benefits of following a refined development roadmap, such as:
• Enabling the identification of key considerations from the outset
• Streamlining the transition between development phases
• Minimising and managing risk
• Using contextual research to drive product requirements and early-stage prototypes
• Accelerating your route to market
We will also discuss the benefits of prototyping in order to prove your proof of principle and proceed through a process of design testing and verification through to transfer to manufacture.