MIF Lunch & Learn 21: Product Design and Regulatory Approval
Companies working in the medtech sector have very specific challenges to face, not least of which is how to design their product. In addition to thinking of things such as usability, look-and-feel, and performance, teams need to also factor in the regulatory approval process, which can influence how your device needs to be designed. Join us to learn from two experts in these respective areas.聽
Josh Abbott聽is Partner and CEO at Tangent Design Engineering, a Calgary-based firm with a 15-year track record developing designs for products in industries ranging from healthcare to aerospace. The company provides a diverse range of services including software support and scale up services.聽Josh has over 20 years of experience in new hardtech product development, and has been involved in technology and product development from napkin sketch to market adoption at scale across many industries, with the goal of creating powerful teams that are aligned to deliver impactful products that improve our world.
Danny Kroo聽is a returning MIF expert. He聽is the founder of Docusys Corporation, which provides聽provides quality management and regulatory affairs consulting to medical device, aerospace, and industrial companies. He founded the company in 1994 and has since worked with hundreds of firms to help them obtain approvals for their technologies.聽
