Pharmaceuticals 2011 - Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies

Why Should You Attend:
Selection of best disinfectants, applying right performance parameters and methods to qualify are keys to designing an effective disinfectant validation program to meet FDA, Irish Medical Board, MHRA, and EMEA scrutiny. This webinar provides guidance on industry trends, regulatory feedback, and keys to design for an effective validation program. Current 483's, Warning Letters, and Field Experiences will be conveyed that allow end users to determine that best methods to validate sanitizers, disinfectants, and sporicides against their isolates. Common pitfalls and issues with validation testing and test methods will be discussed in an effort to improve the overall results.

This Disinfection and Cleanroom Cleaning training will teach you how to choose the best and effective disinfectants, know the different performance parameters for qualifying disinfectants, methods to qualify disinfectants, how to translate results to cleaning procedures, how to writing and execute cleaning procedures.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.