As a medical device company, establishing and documenting your approach to answer these questions can go a long way. More of a policy vs protocol approach.
This is largely where the art of "labeling/claims" comes into play regarding how explicitly worded a "diagnosis" can be. There is a lot of room to play on the spectrum from truly diagnosing a patient with a disease (which requires the most evidence and carries the most liability) all the way down to gently prompting a healthcare provider to look at one record earlier than another one while reviewing their reading queue.