Unlocking the Mysteries of Medical Device Reporting (MDRs) – The Filing, Food and Drug Administration (FDA) Review, and Safety Role of MDRs

Morgan Lewis partner Beth Bierman will be a moderator for this FDLI session on Medical Device Reporting, "Unlocking the Mysteries of Medical Device Reporting (MDRs) - The Filing, Food and Drug Administration (FDA) Review, and Safety Role of MDRs."

The webinar will discuss the structure of the Office of Surveillance and Biometrics and who the FDA "go to" people are and their scope of expertise. Partipants will obtain a better understanding of the MDR regulation, and learn how FDA evaluates and reacts to the information submitted in an MDR report. This webinar should de-mystify the decisions associated with MDR reporting that will enable firms to make timely, consistent decisions associated with MDR event reporting.

When:
Wednesday, February 2, 2011
2:00 p.m.–3:30 pm ET

For more information or to register, please use the above registration link.