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UID:20250811T194156EDT-5675Brm16S@132.216.98.100
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DESCRIPTION:Companies working in the medtech sector have very specific chal
 lenges to face\, not least of which is how to design their product. In add
 ition to thinking of things such as usability\, look-and-feel\, and perfor
 mance\, teams need to also factor in the regulatory approval process\, whi
 ch can influence how your device needs to be designed. Join us to learn fr
 om two experts in these respective areas. \n\nJosh Abbott is Partner and C
 EO at Tangent Design Engineering\, a Calgary-based firm with a 15-year tra
 ck record developing designs for products in industries ranging from healt
 hcare to aerospace. The company provides a diverse range of services inclu
 ding software support and scale up services. Josh has over 20 years of exp
 erience in new hardtech product development\, and has been involved in tec
 hnology and product development from napkin sketch to market adoption at s
 cale across many industries\, with the goal of creating powerful teams tha
 t are aligned to deliver impactful products that improve our world.\n\nDan
 ny Kroo is a returning MIF expert. He is the founder of Docusys Corporatio
 n\, which provides provides quality management and regulatory affairs cons
 ulting to medical device\, aerospace\, and industrial companies. He founde
 d the company in 1994 and has since worked with hundreds of firms to help 
 them obtain approvals for their technologies. \n\nRegistration is now open
 .\n
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SUMMARY:MIF Lunch & Learn 21: Product Design and Regulatory Approval
URL:/innovation/channels/event/mif-lunch-learn-21-prod
 uct-design-and-regulatory-approval-365408
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