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Environmental Monitoring in Pharmaceutical Clean Rooms


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Who should attend?

Microbiology Manufacturing Validation Engineering Maintenance

Details

Overview:
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:
Environmental Monitoring
Microbiology
Manufacturing
Validation
Engineering
Maintenance

Speaker Profile:
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.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Prices

One Dial-in One Attendee Price: US$150.00

Contact

Event Manager
support@compliance4all.com

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