Article

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.

Related Videos
4 experts are featured in this series.
4 experts are featured in this series.
© 2024 MJH Life Sciences

All rights reserved.