Gaining and Re-establishing Control of Your Cleanroom (Recorded)

This webinar will focus on the critical steps in starting up a new cleanroom operation and releasing it for manufacturing. It includes a case study-based approach to dealing with excursion events and establishing control of the cleanroom after a worst case event.

Why Should You Attend:

This webinar will focus on starting up a new cleanroom operation covering everything from utilities to environmental monitoring. Routine cleaning and disinfection will also be covered. Addressing contamination and bringing up the cleanroom after a worst case event will be discussed along with the case studies.

The webinar will further discuss the excursion investigations and troubleshooting parameters and suggestions.

Areas Covered in the Webinar:

• Critical steps in starting a new cleanroom operation
• Critical steps need to release the cleanroom for manufacturing
• Routine cleaning and disinfection strategies
• Utilities
• Contamination
• Environmental monitoring
• Establishing control of the cleanroom after a worst case event
• Excursion events
• Case studies regarding excursion events
• Excursion investigations and troubleshooting parameters

Who Will Benefit:

This 60 minute 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 and environmental monitoring managers