Risk Management is a complicated and contentious topic among medical device professionals. In one corner, there are some who view risk management as a checkbox activity that they have to get done in order to comply with key regulations.
In the other corner, there are QA/RA and product development professionals who are concerned that others don't take this core discipline seriously enough. That's why we surveyed over 300 medical device professionals to learn what risk management looks like in their organization and how they could manage it differently.
In this webinar, you'll learn: