Simplifying Global Compliance
Medical Devices: MDUFA, 510(k) Debate Made List of Top News
Executive Briefing Series
As the year ticked away, it became more clear that the FDA and devicemakers would not be able to compromise early enough to meet the Jan. 15 deadline for a report to Congress that was mandated by the current Medical Device User Fee & Modernization Act (MDUFMA).
To View This Article:
Buy This Article Now
Copyright ©2017. All Rights Reserved.
Design, CMS, Hosting & Web Development :: ePublishing