Companies making software that qualifies as a medical device could one day have access to a special fast-track FDA review pathway, but, first, the agency wants input from stakeholders on what such a pathway should look like. If all goes well, the concept could even be applied to products beyond "software as a medical device" (SAMD).
FDA officials have recently been discussing how to deal with unique challenges of product development faced by makers of SAMDs. The matter has been a strong focus among regulators globally....