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2014 - Sterilization Processes: The Methods, Parameters and Deficiencies Often Cited

Date2014-05-27

Deadline2014-05-27

VenueVirtual Webinar, USA - United States USA - United States

Keywordssterilization method; Medical Device Validation; FDA Violations

Websitehttps://www.onlinecompliancepanel.com/ec...

Topics/Call fo Papers

Instructor: Kenneth Christie
Description:
The sterilization of products or components is achieved through a variety of methods. This webinar will cover the common methods of sterilization, the terminology and the critical parameters associated with each. In addition, this webinar will also highlight recent deficiencies cited by the FDA regarding sterilization methods and their validation. This is a good basic course for those getting involved with performing and understanding sterilization cycles.
Objectives of the Presentation:
Review the common terminology associated with the various sterilization methods
Review the most common methods of sterilization (steam, EtO, dry heat, filtration, gamma)
Discuss the critical parameters monitored for each sterilization method
Review common deficiencies cited with each method reviewed
Who can Benefit:
QA/QC Personnel
Manufacturing
Engineering
Validation
Regulatory
Management

Last modified: 2014-05-23 19:30:30