This site uses cookies. By continuing to use this site you agree to our use of cookies. To find out more, see our Privacy and Cookies policy.
Skip to the content

IOP A community website from IOP Publishing

Browse events




Conference

Reprocessing REUSABLE Medical Devices-Cleaning & Labeling Requirements - Webinar By GlobalCompliancePanel

About this event

Web site
bit.ly/vRQ8D4…
When
7 Dec 2011
Where
Online Training, DE, United States
Organiser
GlobalCompliancePanel
Contact address
webinar web
online training webinar
Suite 1200
Wilmington
Delaware
United States
Tel
800-447-9407
Fax
302-288-6884
E-mail
webinars@globalcompliance…

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 seminar is to explain the rationale, the legal requirements and some methods commonly used for reprocessing & 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 in 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 re sterilized by the user facility, cleaning & sterilization instructions must be precise and validated.

Areas Covered in the Session:
Reasoning behind labeling requirements
Regulatory requirements
Intended use & design
Standards/guidance
Validating cleaning & sterilization
Who Will Benefit:
Design Engineers
QA Manager
Quality Engineers
Regulatory Affairs Manager
Manufacturing Engineers

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884