As an engineer, you're always looking to get more done in less time. In medical device development, however, increasing product complexity and strict regulations like ISO 13485 add pressure. Testing often gets pushed to the end of the cycle, and compressed timelines demand faster delivery.
You can’t afford to rely on scattered, custom-built test setups across teams - they slow you down, increase risk, and delay compliance.
This webinar explores how a modular, universal test architecture can streamline development, reduce rework, and expand test coverage without compromising on product quality. But while the benefits are clear, implementing a modular approach without the right platform comes with challenges - especially around interoperability and scalability.
That’s where NI comes in. We’ll share our medical test expertise and show how our modular hardware and connected software help teams build scalable, future-ready test systems. You’ll see a live demo of test code reuse and hear how one team reduced regulatory compliance timelines using NI’s platform.
Key Learning Objectives
- Architect a modular test system that supports code reuse and scales with your product lifecycle
- Leverage NI’s hardware and software platform to streamline development and reduce rework
- Apply lessons from a real-world case study to accelerate your own test strategy
If you're responsible for designing, developing, or validating test systems for medical devices, this webinar is for you. Register now to reserve your spot!
