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Validating Radiation Sterilization for Medical Device Industries - Webinar By GlobalCompliancePanel

Submitted by Anonymous on Fri, 07/15/2011 - 06:09
08/02/2011 10:00 am
US/Eastern

Gamma and E-Beam radiation has used for sterilization of medical devices for over 50 years. Both methods are validated following the same principles and standards. This webinar will provide an overview of the requirements to validate medical devices for both Gamma and E-Beam sterilization.

Validation is based on the international standard ISO 11137-1:2006 and ISO 11137-2:2006. In this one hour seminar you will obtain a basic understanding of the principles, core requirements of the ISO standard as well as related standards and guidance. We will define how radiation sterilization works, the equipment involved, major issues with product sterilization via radiation, and the validation requirements. Routine process control and monitoring will be reviewed along with requirements to maintain the process effectiveness.

Why should you attend:
Radiation sterilization validation is a topic that results in many audit observations from the FDA and international regulatory bodies. Proper understanding of the principles and requirements of the related standards is crucial to proper compliance. In addition, understanding the requirements and integrating them early in the product design can lead to quicker time to market. This seminar will help RA/QA staff understand the basic principles as well as the standards and regulations. This will be useful when reviewing validation plans, performing internal audits and dealing with regulators. It is also beneficial to R&D staff to understand the requirements so they may be incorporated into the design inputs correctly.

Areas Covered in the Session:
Introduction
Terminology / Definitions
Radiation characterization / effectiveness
Process Equipment
Product and Material Issues
Process Definition
Validation IQ/OQ/PQ
Documentation, review and approval of validation
Routine Monitoring
Product Release
Maintenance of process effectiveness
Who Will Benefit:
RA Directors, Managers and Staff
QA Directors, Managers and Staff
Internal Audit Staff
R&D Directors, Managers and Staff

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

1000 N West Street | Suite 1200 | Wilmington | DE

Zip 19801

Webinar Presenters: 
global compliance panel
Webinar URL: 
global compliance panel
Your rating: None
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Tags:
  • documentation
  • Medical Device Industries
  • Radiation
  • review and approval of validation
  • Sterilization
  • Validation
  • Validation IQ/OQ/PQ
  • webinars


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