In this interview, Frank Panofen, PhD, and Daniele Pandolfi of Particle Measuring Systems (PMS) discuss the following cleanroom contamination monitoring monitoring topics:
- Viable monitoring in pharmaceutical manufacturing
- Risk-based approach to monitoring methodology and design, cleanroom classification and cleanroom qualification
- Continuous sampling meaning and applications
- Active air sampling and real-time testing
- Changing regulatory expectations for pharmaceutical manufacturers
Learn more about cleanroom monitoring regulations:
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More Cleanroom monitoring system insights
Ongoing Monitoring – Choosing the Most Suitable Particle Sample Point Locations in the Cleanroom
Effective Risk Assessment in Pharmaceutical: Steps to Ensuring a Successful Audit
Microbial Environmental Monitoring: Managing Auditor Expectations
Get solutions for your cleanroom monitoring:
- airborne particle counting (remote and mobile)
- microbial contamination monitoring (remote and mobile)
- facility monitoring
- data management solutions
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Relevant Cleanroom Monitoring System Videos
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