Medical device manufacturing demands precision, standardization, and seamless cross-functional collaboration. This session explores proven SOLIDWORKS best practices and workflows used in the medtech industry to streamline product development and ensure compliance with strict regulatory standards.

Attendees will learn how to leverage tools such as Drafting Standards, Compare Utility, and Macros to build repeatable, validated design processes covering techniques to work and study components, drawings, part details and more. We’ll look at these techniques to drive consistency across engineering teams.

Drawing from five years of hands-on experience in regulated product design, this session demonstrates tools that can improve standardization, accelerate design reviews, improve communication, and enhance regulatory readiness, giving you methods to be consistent by design.

Join Zoom Meeting

https://us06web.zoom.us/j/86119932346?pwd=TShIGnxvRVZlaLNBGWa0cebzxI6FZF.1

Meeting ID: 861 1993 2346

Passcode: 261887

THIS EVENT WILL NOT BE RECORDED FOR RELEASE