In 1996 when the FDA first required that companies implement design controls for medical devices, the process was much simpler. Today, we have to include risk management activities, software verification and validation, usability engineering, and cybersecurity. This adds dozens of new tasks in your design and development plan. The good news is that we have modern software tools that can help you create a medical device design plan in minutes. In our Friday live-streaming video, we will show you how to create your own step-by-step in less than 30 minutes.