Meeting the Challenges of Medical Device and Technology Design
QNX Software Systems, in partnership with MPC Data and ARM, is hosting a one-day seminar entitled “Medical Devices & Technology: Design for Regulatory Compliance” - in Cambridge, UK.
Increased regulatory scrutiny in the approval process and growing
complexity of software and hardware technology in the design/development phases are impacting medical device manufacturers’ ability to bring new, innovative devices to market within the window
required for maximum adoption.
Join us for this one-of-a-kind seminar as our technical experts discuss how the right technology building blocks and planning/best practises for achieving regulatory compliance assist manufacturers of medical devices and other safety or security related devices achieve regulatory compliance much sooner, and with far less risk of costly recalls and/or misuse after deployment.
The seminar is being held for design managers and engineers, product and project managers and software developers and engineers in companies planning to design and build equipment for the healthcare and medical market.
Guests will have an opportunity to hear insights from industry thought-leaders, see innovative technology demonstrations and network with colleagues from a variety of companies.