4-Hour Virtual Seminar on Aseptic Processing and Validation 2019

Topics

• Facility and personnel requirements necessary to maintain microbial control
• The difference between Aseptic and Bulk processing
• The gowning requirements associated with different cleanroom classifications
• Basic principles of microbiology and microorganism recovery in relation to cleanroom environmental monitoring (EM) and impact to product
• The purpose of media fills, and elements critical to their success
• Basic principles of aseptic processing, including:
• Ways that they can impact/ improve site-specific EM and aseptic behavior issues
• Behaviors that are or are not appropriate when working in controlled areas, and why

Who should Attend

• Quality Control Department Management and Staff
• Quality Assurance Department Management and Staff
• Records Managers
• Operations Department Management and Staff
• Engineering Department Management and Staff
• Production Management and Staff
• Facilities / Maintenance Management and Staff
• Validation Management and Staff