Jeff Shapiro presented at the FDLI 2014 Medical Device Conference – Key Legal and Regulatory DevelopmentsMedical Device Reporting (MDR) requirements and the Appeals Process.
WhenFebruary 12, 2014
At the Food and Drug Law Institutes (“FDLIs”) 2014 Medical Device Conference – Key Legal and Regulatory Developments, which will take place in Washington, D.C. on February 27, 2014, top FDA officials will discuss their most significant recent activities and forecast upcoming medical device activities. Experts will analyze the most important cases of 2013 and predict what legal and policy developments to expect in 2014. In addition, panelists will analyze pressing compliance issues, including regional warning letters and off-label promotion issues. This conference will cover hot topics in the medical device realm, including mobile medical apps, combination products and the Sunshine Act.
Hyman, Phelps & McNamara’s Jeffrey K. Shapiro will present with CDRH Ombudsman David Buckles, PhD, FACC in a session covering two FDA guidance documents issued last year – one on Medical Device Reporting (“MDR”) requirements and the Appeals Process
To register for the conference and to obtain additional details, please go to the FDLI website. FDA Law Blog readers can obtain a discount by using the code MEDDEV14.