FDA Reviewing Fewer Generic Applications and Tentative Approvals Take Longer
The FDA’s latest quarterly snapshot of the agency’s GDUFA II performance shows fewer abbreviated new drug applications (ANDAs) under review than for the same time last year and that the agency is taking much longer to issue tentative approvals.
To View This Article:
Login
Subscribe To FDAnews
Upcoming Events
MAGI@home Clinical Research Conference 2024
Featured Products
- From QSR to QMSR: Meeting FDA’s New Requirements" width="" height="" />
From QSR to QMSR: Meeting FDA’s New Requirements
Laboratory Developed Tests" width="" height="" />
FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule