Report: CDER is Meeting User Fee Goals but Struggling With Biosimilar Application Targets

By Sam | March 18, 2021

The FDA approved 17 original abbreviated new drug applications (ANDAs) in the third quarter of fiscal 2020, 14 in the fourth quarter and 18 in the first quarter of fiscal 2021. It’s seen a downward trend in manufacturing supplements for new drug applications (NDAs), biologics license applications (BLAs) and ANDAs, approving 314 in the third quarter of fiscal 2020, 277 in the fourth quarter and 149 in the first quarter of this fiscal year.
Source: Drug Industry Daily

Posted in Drug Industry Daily