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Medical Device 2012 - Application of CAPA to the Device Sterilization Process

Date2012-03-15

Deadline2012-03-14

VenueHyatt Rege, USA - United States USA - United States

Keywordsmedical device sterilization; FDA; EO sterilization processes; CAPA; Validation processes; EO Validation; Radiation Process and Validation; Critical and noncritical deficiencies

Websitehttp://www.complianceonline.com/ecommerc...

Topics/Call fo Papers

Do you use a Contract Sterilizer for your medical device sterilization? Are you not an expert in industrial sterilization? If you answered “yes” to either of these questions, this seminar is a must for you and your team members.


The FDA and your Notified Body will look to you, the medical device manufacturer, for the answers to deficiencies in the sterilization process whether sterilization is performed at your location or at a contract sterilizer.


Who will benefit
This course benefits anyone involved in ensuring quality for medical devices and is ideal for quality and engineering professionals working in the medical device sector.
- QA personnel
- CAPA team members
- SA personnel
- Quality Engineers
- Operations Managers

Last modified: 2012-02-14 16:37:59