We're a medical device company, so we need to do ISO13485 quality assurance processes on changes to software and hardware.
I had already been thinking of using an LLM to help ensure we are surfacing all potential concerns and ensure they are addressed. Partly relying on the LLM, but really as a method to manage the workflow and confirm that our processes are being followed.
Any thoughts on if this might be a good solution? Or other suggestions by other HN users.