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June 1, 2018 - December 31, 2019

Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements

United States

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Event Details

Begins: June 1, 2018

End: December 31, 2019

Event Location: United States

Website: https://www.compli..0831-prdw

Event Organizer

Event Organizer: ComplianceOnline

Contact Person: Sreeraj Mathilassery

Phone Number: +1-888-717-2436

Website: https://www.complianceonline.com/

Overview

This training program will explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices.

Why Should You Attend:

Any firm reprocessing another manufacturer's medical device becomes the legal manufacturer with all the responsibilities for compliance, especially sterility. Failure to prove sterility is almost certainly a cause for either voluntary recall or FDA mandated recall. The same is true if you are reprocessing your own medical device. If intended to be resterilized by the user facility, cleaning and sterilization instructions must be precise and validated.

Much attention has been paid to the regulatory requirements of reprocessing single use devices. However, there is increasing attention being directed towards reprocessing reusable medical devices and regulatory requirements.

The purpose of this webinar is to explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices.

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