Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies (Pharmaceuticals Trai)
Venue: Online Event
|Event Date/Time: Apr 14, 2011||End Date/Time: Apr 14, 2011|
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.
NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.