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.
International Drug and Device Recalls: the 90-minute FDAnews webinar that shows you how to craft a master global
recall strategy to protect your product from the toughest regulatory storms, at home and abroad — solidly based upon the regulations of the FDA,
World Health Organization, European Medicines Agency and the Health Protection Branch of Health Canada.
Audio CD/Transcript - March 24, 2010 The Audio CD/Transcript will be shipped the week of April 19, 2010.