|Articles|February 1, 2003
Legislation: New FDA law streamlines device review, approval process
Baltimore-Legislation signed Oct. 26, 2002 promises to expedite the FDA device review and approval process. Developed in concert with industry, the Medical Device User Fee and Modernization Act of 2002 (MDUFMA) has strong bipartisan support.
Advertisement
Newsletter
Don’t miss out—get Ophthalmology Times updates on the latest clinical advancements and expert interviews, straight to your inbox.
Advertisement
Latest CME
Advertisement
Advertisement
Trending on Ophthalmology Times - Clinical Insights for Eye Specialists
1
FDA approves Rayner’s RayOne EMV Toric intraocular lens
2
Avisi Technologies’ investigational device exemption for VisiPlate approved by FDA
3
NeuroOp Guru: When proptosis isn’t thyroid eye disease
4
Ophthalmic innovation by the decades: The 1980s and 1990s
5