Amp 2024 Usfda. The us fda has granted fast track designation to amplia's lead drug. You may submit an abstract and apply to join amp on the same day, up to and through the submission deadline, however, we encourage you to join amp in advance of the.
The products in each list contain information about what. The manufacturer and user facility device experience (maude) database is a searchable database of medical device reports (mdrs) of adverse events involving medical devices.