Tuesday, September 24, 2013 |
01:00 AM Eastern Daylight Time |
Please join us for a one-hour webinar to discuss the FDA's new draft guidance on Medical Device Reporting (MDR) requirements as well as an interactive Q&A on everything you always wanted to ask about MDR.
Topics will include:
When:
Tuesday, September 24
12–1 pm ET
Presenters:
M. Elizabeth Bierman | Partner, Washington, D.C.
Michele L. Buenafe | Associate, Washington, D.C.
CLE Credit:
CLE credit in FL, IL, NJ, NY, PA, TX, and VA is currently pending approval.