PDUFA Proposal Sheds Tier 3 Funding
You may also be interested in...
E-Submission Part Of FDA Reg Reform Plan; Alzheimer’s Data Standard About To Debut
Standards for organizing clinical data from research in some major diseases are taking shape as FDA moves to clear a regulatory path that eventually could allow all submissions to be done electronically.
E-Submission Part Of FDA Reg Reform Plan; Alzheimer’s Data Standard About To Debut
Standards for organizing clinical data from research in some major diseases are taking shape as FDA moves to clear a regulatory path that eventually could allow all submissions to be done electronically.
Burr Warns User Fee Renewal Could Be Difficult Without Performance Measure Improvements
Senator tells FDA Commissioner Hamburg that time to market is important metric during hearing dominated by questions about medical device review.