Join us for a live interview with Bryce Rutter, a leading expert in the design of medical devices. Attendees will get an inside look at how he approaches the device development process during this keynote session.
A crucial hurdle for all medical devices to pass during development is completing a successful biocompatibility testing battery. Many delays are caused by an incomplete understanding of what biocompatibility endpoints a device must pass. This presentation will cover the foundation of biocompatibility testing and how to create an efficient testing plan to save you time and money, allowing you to reach patients faster. During this presentation the following topics will also be covered: ISO 10993s latest revision and what has changed Understanding test article needs and proper sample preparation Case Studies
In a panel hosted by Greenberg Traurig, participants will discuss how M&A, IP and products liability trends are impacting medtech. Attendees can expect to learn about: Mergers & Acquisition (M&A) and Intellectual Property (IP) trends Products liability litigation – what every medtech company needs to know