Description
My team developed software that was used as part of a medical product. We used modern development practices and tools to document the code and the APIs exposed by our microservices, but was that enough?
This talk introduces the audience to the particularities of developing medical device software and the regulatory landscape that you must comply with. I’ll focus specifically on the processes and culture that enables the creation of medical software device documentation intended for auditors, without damaging (too much) the team velocity and spirit.