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On Demand

Applying ISO 14644-21 Airborne Particle Sampling Techniques: Classification vs Monitoring and Instrument Selection on demand webinar

A central theme of the new ISO 14644 Technical Report 21 (TR 21) focuses, in section 4.0, on the difference between cleanroom classification and monitoring, this presentation will review the core differences between these points and associated instrumentation choices described in section 5.2 that best meet these needs. Classification is centered on the quality of the measurement and the best, most accurate measurement that can be taken when considering instrumentation differences; monitoring is a function of measurement over time, so the quality of the data becomes key, which may require different instruments for understanding the changes to ‘normal’ conditions.

What you’ll learn:

  • Introduction to the new ISO 14644 Technical Report 21
  • Understanding the difference between classification and everyday cleanroom monitoring
  • Instrumentation choices associated with the regulatory needs
  • Ensure data quality by understanding changes to normal conditions

Who should attend:

  • QA & QC
  • Production and manufacturing teams
  • Environmental monitoring experts
  • Biologists
  • R&D team
  • Biopharmaceutical engineers
  • Automation managers
  • Regulatory experts

 

Webinar Presented By:
Mark Hallworth
Global Pharma and Sr. GMP Advisor, Life Sciences Division

Mark Hallworth is a globally recognized authority in pharmaceutical contamination control, specializing in the design, validation, and implementation of GMP-compliant environmental monitoring systems. With decades of experience, he has led more than 200 projects across cleanroom facilities, focusing on regulatory compliance, data integrity, and system performance. Mark has contributed to the development of particle counters for hazardous environments and 21 CFR Part 11–compliant software for batch release and test management. He has authored over 100 technical papers and contributed to leading industry publications and reference books. Mark frequently presents at international forums, including the Parenteral Drug Association (PDA) and ISPE, where he teaches best practices in cleanroom monitoring and GMP compliance. Additionally, Mark served on the ISO 14644-21 technical committee and received the IEST James Mildon Award for advancing knowledge in contamination control. His work continues to shape standards and practices across the global pharmaceutical and biotechnology industries.

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