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GMP Environmental Monitoring for Pharmaceutical Clean Rooms

 
  February 01, 2021  
     
 
ComplianceOnline, online event
16 February 2021


Areas Covered in the Webinar:

  • GMP Compliance of Clean Room Environment
  • Regulatory Clean Room Classification and Requirements
  • Environmental Monitoring Program
  • Action and Alert Levels
  • Non-Viable Particulate Monitoring Systems
  • Microbial Monitoring Systems
  • Personnel Gowning and Aseptic Practices in Clean Room
  • Clean Room Monitoring Practices - Frequency, Locations, and Investigations
  • Product Release
  • Environmental Monitoring Data Trend reports
 
 
Organized by: ComplianceOnline
Invited Speakers:

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 35 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. Roger has taught courses in microbiology at Seneca College (Pharmaceutical Technology Program) in Toronto, Canada.

Roger's areas of expertise include: aseptic pharmaceutical manufacture, GMP facility audits, technical transfer, microbiology, environmental monitoring/contamination control, product sterilization, process development, process validation, clinical supply manufacturing, labeling and distribution, US / International regulatory requirements, regulatory submissions, and quality assurance/control.


 
Deadline for Abstracts: 14-2-2021
 
Registration: https://www.complianceonline.com/gmp-environmental-monitoring-for-pharmaceutical-clean-rooms-webinar-training-705783-prdw?channel=hum-molgen
E-mail: referral@complianceonline.com
 
   
 
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