The 4-Hour Virtual Seminar on Aseptic Processing and Validation 2019 is a webinar that covers topics such as:
- 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
The 4-Hour Virtual Seminar on Aseptic Processing and Validation 2019 is intended for:
- 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
