In the medical devices field we have standards like ISO 13485 and IEC 62304. They are very broad and high-level standards and require a lot of interpretation. What would REALLY help small companies that are just getting started, is a line by line explanation of what you need to do, why, and what possible solutions there are. I'm not sure, but I believe doing so could violate the copyright. Even the fact that I'm not sure prevents me from doing it.
Yes, and each one will tell you something different ;) I much prefer open discussion where the best ideas stay afloat and bad advice can be publicly shamed.
