This webinar will take you through the discussion of how environmental monitoring data is reviewed for product release, also this session provides meaningful information on the quality of the aseptic processing environment.
Why should you Attend:
This webinar first explains the various US and international regulatory requirements for the various clean room classifications as well as the environmental monitoring of clean room environments. Next, the presentation details the benefits, the regulatory requirements and the testing requirements for a comprehensive Environmental Monitoring Program.
Areas Covered in the Session:
Regulatory Clean Room Classification and Requirements
Environmental Monitoring Program
Action and Alert Levels
Non-Viable Particulate Monitoring Systems
Microbial Monitoring Systems
Who Will Benefit:
Roger Cowan is the founder and owner of R Cowan Consulting Services LLC, a consulting company specializing primarily in the area of pharmaceutical contract manufacturing. He has 37 years experience in pharmaceutical quality assurance and manufacturing. In his career, Roger has held various manager / director positions in Quality Assurance, QC Laboratory, Technical Services Validation, Manufacturing, and Clinical Supply manufacturing and distribution.
One Dial-in One Attendee Price: US$150.00