Medical Devices

Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling Final Guidance - March 24, 2015

Summary:
On March 12, 2015, the FDA published a final guidance on reprocessing reusable medical devices. This guidance is a step toward further reducing the risk of patient infection by providing manufacturers with recommendations to validate their reprocessing instructions to ensure devices remain safe and effective for reuse.

The goal of this webinar is to help manufacturers understand the recommendations described in the final guidance.

Following a brief presentation, the FDA will respond to manufacturers’ questions regarding the final guidance document.

Webinar Details:

No Registration Needed

Date: Tuesday March 24, 2015
Time: 1:00 -2:30 PM, Eastern Time (please connect by 12:45 PM)

To hear the presentation and ask questions:
Dial: 888-324-3908; passcode: 7495402
International: 1-312-470-7226; passcode: 7495402

To view the slide presentation during the webinar:
https://www.mymeetings.com/nc/join.php?i=PW2984280&p=7495402&t=c

We added an additional link to ensure that every participant is able to log in to the webinar. If you receive an error message while using the first link, please use the following link to obtain access to the live presentation:
https://www.livemeeting.com/cc/events_vbc1/join?id=PW2984280&role=attend&pw=7495402

Following the webinar, a transcript, recording and slides will be available at: http://www.fda.gov/CDRHWebinar. The slide presentation will be available at this site on the morning of the webinar.

Note: The FDA does not provide Continuing Education Credits (CEU) or Certificates of Attendance for webinar attendance.

Target Audience: Manufacturers of reusable medical devices

Page Last Updated: 04/01/2015
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