Sept 26 Minneapolis | Sept 28 San Diego
The need to harden cybersecurity is at an all time high. The FDA agrees. Recent (March 2023) regulations from the agency now require manufacturers to submit specific cybersecurity documentation with each 510(k) filing; without this, applications will be categorically rejected. The FDA also outlines the expectations for device manufacturers regarding cybersecurity throughout the product life cycle, including risk management, design controls and post-market surveillance. This half-day session is designed to help you better understand and comply with this new guidance, and propel you on your medical device cybersecurity journey. Register Now >>
August 24, 1 pm EDT — The Rust programming language has been gaining traction in the past few years, as it is known for its performance, safety and memory management. Join our webinar and to find out if Rust is right for your next software project. Register Now >>
September 14, 1 pm EDT — Join us for the second installment of our webinar series, during which we explore the interesting and controversial aspects of quality and test solutions used in engineering for medical devices. Register Now >>
Choosing a toolkit for your GUI? Here's a handy resource that compares 10 popular frameworks to aid in your decision making.
Discover how ICS addressed a tricky customer requirement around dual displays. Read More >>
Join ICS at NXP Technology Days, NXP's global training program that offers engineers step-by-step instruction, in-depth lectures, and hands-on workshops led by experts addressing topics across automotive, mobile, smart home, communication infrastructure, and industrial markets. Learn More >>