Regulatory Science Series: Medical Device Regulation

Date: 
April 20, 2018 - 12:00pm - 2:00pm

Join us for a panel on Friday, April 20, from 12:00 p.m. to 2:00 p.m. with Maureen Dreher, PhD, Policy Analyst in the Clinical Trials Program at the FDA’s Center for Devices and Radiological Health (CDRH), and Heather Vander Ploeg, MBA, CCRA, Clinical Operations Manager at Regenesis Biomedical. Dr. Dreher is a biomedical engineer and has been with the FDA since 2007 as a researcher and subject matter expert on medical devices. Ms. Vander Ploeg brings extensive industry experience in medical device development, including clinical trial management at Medicis Pharmaceutical prior to joining Regenesis.  Please join us for an engaging discussion featuring FDA and industry perspectives on the regulation of medical devices. Lunch is included with your RSVP! 
 
To RSVP, please visit:  https://uarizona.co1.qualtrics.com/jfe/form/SV_cUy62lUXMP3kuPz