David’s topic is A Canadian Perspective of Device Innovation in MedTech: From Concept to Commercialization
The learning objectives from his presentation are:
- How to use standards to help you meet the requirements of the medical device regulations
- Why adopting a risk-based approach is the key to successful medical device development
- The importance of understanding user needs and the application of usability engineering
David is a director at eg technology with extensive experience in the compilation of technical files and regulatory requirements for software development of CE marked and FDA approved medical devices. He provides overall monitoring, reporting, delivery, and strategic planning of projects. Skilled at leading multidisciplinary engineering teams, he is the technical lead for projects using his experience to solve specific challenges and to set the overall technical direction of the development. His expertise includes the application of standards, design specifications and testing at all stages of the product development cycle.
David has an overall responsibility for the management of new and existing client accounts. He works closely with the senior management team to evaluate business operations and strategy for the consistent business development and growth of eg.
David has been with eg technology since 2008 and was appointed as a director of the company in 2019. Prior to this, David forged a career in software engineering and product development in the MedTech and BioTech sectors. He holds an MBA and Diploma in Economics from the Open University following his degree in Computer System Engineering from the University of Warwick.