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DTSTART;TZID=UTC:20230615T000000
DTEND;TZID=UTC:20230615T000000
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SUMMARY:SEMINAR:  What’s New in Product Development Software | Montréal\, QC
DESCRIPTION:Discover the New Technology Available in Dassault Systèmes’ Product Development Software\n  \nJoin us for an in-person event to learn about the latest capabilities in Dassault Systèmes’ software solutions that support your evolving product development needs – from design and simulation to manufacturing and product lifecycle management (PLM). \n  \n \n  \nJune 15\, 2023   |   1:00 pm – 5:00 pm ET\nFollowed by Networking Reception – REGISTER BELOW\n  \nDiscover how the impossible has become possible in the last few years. See how Dassault Systèmes’ ever more powerful and easy-to-use applications and 3DEXPERIENCE platform can elevate your product development efficiency and innovation to the next level. Also get the opportunity to network with your peers and experts from Inceptra and Dassault Systèmes. \n  \nThis seminar will provide insights and demonstrate the latest capabilities and enhancements to: \n  \n[TABS_R id=21928] \n  \nDATE:   June 15\, 2023 \nTIME:   1:00 pm to 5:00 pm ET \nLOCATION:   Dassault Systèmes \nADDRESS: \n393 Saint-Jacques\, #300\, Room Armand Bombardier\, Montréal\, QC H2Y 1N9 \nAGENDA: \n1:00 pm – 1:15 pm        Registration \n1:15 pm – 5:00 pm        Presentations & Demonstrations \n5:00 pm – 7:00 pm        Networking – Appetizers & beverages will be served \n  \n\n  \nRegister Now!
URL:https://www.inceptra.com/event/seminar-whats-new-in-product-development-software-montreal-qc/
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DTSTART;TZID=UTC:20230621T000000
DTEND;TZID=UTC:20230621T000000
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LAST-MODIFIED:20240919T192115Z
UID:10000036-1687305600-1687305600@www.inceptra.com
SUMMARY:WEBINAR: Easily Shift from Traditional MedTech Product Design to Modeling and Simulation
DESCRIPTION:LIVE WEBINAR\n  \nUnified Modeling and Simulation (MODSIM) is providing a new paradigm for MedTech product design \nCurrent MedTech product design methods struggle to meet the demand for rapid\, safe\, and effective therapeutic solutions that pass regulatory scrutiny. The FDA has been promoting the use of Computational Modeling & Simulation (CM&S) to address this challenge. \nHowever\, obstacles remain in fully harnessing CM&S due to regulatory processes and barriers faced by medical device manufacturers\, such as legacy processes\, vendor selection\, and implementation decisions. \n  \n \n  \nJune 21\, 2023   |   10:00 am – 11:00 am ET\nRegister Now \n  \nIn this presentation\, learn how to easily implement a virtual (in silico) MODSIM approach. This will help to better manage the conflicting needs for usability\, manufacturability\, and cost in MedTech product design engineering and validation process. \n\nSee the power of Modeling and Simulation (MODSIM) to dramatically optimize design performance and speed development of innovative medical devices\nLearn how MODSIM builds on the concept of “left-shifting” to increase the impact of simulation on engineering and design\nHear an example of designing a drug delivery combination device and discover how designers\, engineers\, and analysts are able to\ncollaborate on making performance-based decisions to validate optimal designs against regulatory requirements and business objectives\n\n  \nRegister Now \n 
URL:https://www.inceptra.com/event/webinar-easily-shift-from-traditional-medtech-product-design-to-modeling-and-simulation/
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