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.
In this 90-minute webinar, noted attorneys Holley Lutz and Lisa Murtha discuss the Medicare Clinical Research Coverage Policy — how to negotiate a clinical trial budget that keeps your sites operating and billing in compliance. Learn which costs are billable to third-party payers and why sites have trouble billing appropriately.
Audio CD/Transcript - Nov. 9, 2010
The Audio CD/Transcript will be shipped the week of Dec. 6, 2010.