In the medical device industry, risk management is not just a regulatory requirement. It is a fundamental practice to ensure the safety, effectiveness and quality of devices that directly impact pati...
...nhance your product safety with FMEA, please check out our recent blog post on how hazard analysis and FMEA relate to each other. To Recap: Hazard Analysis Essentials: Understand what hazard a...
Your medical device software is likely to contain a number of components, items, packages, libraries, etc. not developed directly by your company. It may include open-source or purchased software. Un...
Copied to clipboard