June 21st 2017 MSCE Meeting
June 21st 2017
TIME: 5:00 PM
PRESENTER: Jahan Azizi
TOPIC: Improving Patient Safety by Reporting Problems with Medical Devices through the FDA Medical Device Safety Network (MedSun) and MedWatch.
This presentation will cover:
Identification of several types of medical devices
Why reporting problems with medical devices is important
Your role in reporting within your healthcare facility and in promoting patient safety with medical devices
Steps to take to report an adverse event or other problem with a medical device
ROOM: Administration Building West, 1st Floor Private Dining Room
Hospital: Beaumont Hospital Royal Oak
ADDRESS: Beaumont Hospital, 3601 West 13 Mile Road, Royal Oak, MI 48073
There is no cost for this program, and no cancellation fee. The US Food and Drug Administration/CDRH/OSB/DPSP, as a provider approved by the California Board of Registered Nursing, Provider Number CEP 16323, grants 1.25 contact hours of Continuing Education credit for this program.
Please fill out the evaluation form and return it to medsun@fda.hhs.gov by July 21, 2017 (one month after the program) to receive a CE certificate from FDA’s MedSun Program.