Report shows how the FDA incorporates the two ISO standards in its medical device development policy, how the EU version of the two standards differs in significant ways and how the EU Medical Device Regulation may require further changes in the European standards.
Mark your calendar for Wednesday, March 31, 2010, when Dr. Schiff makes an exclusive appearance on your desktop screen, courtesy of FDAnews.
In a fast-paced 90-minute webinar, he’ll disclose problem areas and arm you in advance with eight strategies to make sure you get
a clean report.
Audio CD/Transcript - March 31, 2010
The Audio CD/Transcript will be shipped the week of April 26, 2010.