Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment

This 90-minute webinar on Disinfection and Cleanroom Cleaning will cover effective ways to rotate disinfectants, most current industry methods for applying disinfectants and effective methods for controlling residues.

Why Should You Attend:

Designing an effective cleaning and disinfection program is a critical part of your facility operations and contamination control program to meet FDA, EMA, and MHRA regulations. This process involves selecting the most effective products against your isolates, rotating these products, and having a safe and effective method to apply these products. oday end users typically struggle with how often to rotate products and determining exactly which products to rotate.

Areas Covered in the Seminar:

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

Who Will Benefit:

This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs, including companies in the Pharmaceutical, Biotech, and Medical Device fields. The employees who will benefit include:

• QA and QC Managers
• Disinfectant Validation Managers
• Operations Managers
• Cleanroom Managers
• Personnel and contractors that clean and disinfect cleanrooms
• EH&S Managers
• Regulatory Compliance Managers & Environmental Monitoring Managers