Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment 2012

• The need to control bioburden involves a sound cleaning and disinfection program
• Effective ways to rotate disinfectants
• Effective methods for controlling residues
• The most current industry methods for applying disinfectants
• All the necessary components will be discussed that will allow end users to be in compliance with FDA and EMEA

Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment 2012 brings together attendees from Pharmaceutical, Biotech, and Medical Device fields and other FDA and EMEA regulated companies including Disinfectant Validation Managers, QA and QC Managers, Cleanroom Managers, Operations Managers, EH&S Managers, Personnel and contractors that clean and disinfect cleanrooms and Regulatory Compliance Managers & Environmental Monitoring Managers.