In this Ethylene Oxide (EO) Sterilization training, you will learn how to evaluate your sterilization process for cost reduction/process efficiency, and also learn how to implement such changes without jeopardizing product safety and regulatory compliance.
Why Should You Attend:
Many medical device manufacturers are not taking advantage of latest sterilization technologies and knowledge to effectively reduce the sterilization process cost. This is due mainly to: lack of knowledge of latest technologies, fear of getting out of regulatory compliance or belief that changes to the sterilization process are too complex or risky.
In this session, you will acquire the knowledge to evaluate your sterilization process for cost reduction, and learn how to implement such changes without jeopardizing product safety and regulatory compliance. Analyzing the microbiological and EO residual aspects of your cycle with a different approach will result in re-engineering it for cost reduction and avoidance while complying with EN/ISO11135.
Date: August 31, 2012
Time: 10:00 AM-11:00 AM PDT
Cost: $249 per attendee per computer terminal
Registration: SIgn-Up on-line now. Add to your shopping cart.
Added by complianceonlinecom on August 8, 2012