Unified Modeling and Simulation (MODSIM) is providing a new paradigm for MedTech product design
Current 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.
However, 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.
June 21, 2023 | 10:00 am – 11:00 am ET
In 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.
- See the power of Modeling and Simulation (MODSIM) to dramatically optimize design performance and speed development of innovative medical devices
- Learn how MODSIM builds on the concept of “left-shifting” to increase the impact of simulation on engineering and design
- Hear an example of designing a drug delivery combination device and discover how designers, engineers, and analysts are able to
collaborate on making performance-based decisions to validate optimal designs against regulatory requirements and business objectives