I did for non-invasive devices that were mostly class I + II. Even for those 1-2 years is very fast. Larger manufacturers might be quicker, but it is the time y

I did for non-invasive devices that were mostly class I + II. Even for those 1-2 years is very fast. Larger manufacturers might be quicker, but it is the time you should calculate with at minimum. I think the state of emergency allows to cut the time short, because these are very short time frames for clinical trials.