SILVER SPRING, Maryland – The post-approval study (PAS) is one of the most frustrating parts of the development process for makers of novel devices, not just because patients are not particularly eager to enroll. (Medical Device Daily)

WASHINGTON — The second day of this year's annual meeting of the Medical Device Manufacturers Association (MDMA; Washington) covered a couple of hot-button topics, and a session that got the audience's rapt attention was one that dealt with compliance issues in an era of increasing governmental scrutiny. (Medical Device Daily)

WASHINGTON – Dan Schultz, MD, director of the Center for Devices and Radiological Health at FDA, gave a brief address at this year's annual meeting of the Medical Device Manufacturers Association (MDMA; Washington), and had a lot to say about a lot of things. (Medical Device Daily)