The Biomedical Consortium is pleased to offer a January 9, 2012 workshop on the subjects of dealing with medical device complaints and required MDR reporting to the FDA.

Presenters will be Richard Roy, Senior MDR Manager, Medtronic CRDM, and Milissa Michurski, Compliance Officer, Minneapolis District, FDA.  Sharon Kapsch, MDR Division, CDRH, has been invited for a call-in.

Take advantage of this great opportunity for workshop participants to find out what the medical device industry should be doing about complaints and what is required by the FDA.

Registration closes Friday, January 6th.  For more information and to register: http://mnasq.org/spotlight/complaints-mdr-workshop/