UNITED STATES info@pmeasuring.com +1 303 443 7100
UNITED KINGDOM info.uk@pmeasuring.com +44 01733 454 207
IRELAND info.ie@pmeasuring.com +353 1 295 7373

Optimizing Monitoring: The Science of Particle Loss

Duration: 1h
When? November 19, 2025
Register here:

Particle loss in sample tubing recently gained new visibility with the changes to EU GMP Annex 1, requiring that all tubing, used for particle counter applications, be “qualified”. The understanding of tubing losses forms a foundational component in how the data can be transformed into useful information and applied to the site Contamination Control Strategy (CCS), through improved, timely, responses to alert and action events, and quality decisions.

This webinar presents study results from guidance presented in ISO/TR 14644-21, and testing conducted using traceable instruments and particle sizes across varied configurations. Key variables: tubing length, number of bends, internal diameter, and material—were systematically evaluated to assess their influence on particle transit in controlled environments.

Findings highlight changes in sampling setup significantly impact particle transmission efficiencies, particularly for larger particles and more complex configurations. The results support a risk-based approach to system qualification and emphasize the need for configuration control to meet evolving regulatory expectations regarding data traceability and integrity. As regulatory agencies increase scrutiny on environmental monitoring systems, understanding these variables becomes essential for designing defensible monitoring strategies.

This presentation offers guidance for optimizing sampling configurations and enhancing compliance, through a better understanding of the variables and resulting data.

What you'll learn:
  • A clear understanding of how system configuration impacts particle recovery
  • Evidence-based guidance on optimizing sampling setups to reduce loss
  • Tools to evaluate and document environmental monitoring systems for compliance
  • Insights aligned with ISO 14644, Annex 1, and Pharma 4.0 principles
  • A practical checklist for assessing risk in particle monitoring setups
Who should attend:
  • QC (micro managers and/or supervisors)
  • QA (on the floor for filling lines)
  • Project Managers
  • QP and Plant Managers
  • Production Supervisors and Managers
  • Engineering (MS&T Engineers)
Duration: 1h
When? November 19, 2025
Register here:
Webinar Presented By:
Mark Hallworth
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.

Luca Calisi
Luca Calisi
Advisory Specialist

Luca is an Advisory Specialist in the Global Sterility Assurance Team at Particle Measuring Systems, with extensive experience in pharmaceutical microbiology, contamination control, and environmental monitoring. He began his career in microbiological quality control and now focuses on contamination control strategies, risk-based solutions, and sterility assurance for GMP manufacturing. Luca supports global pharma companies with risk assessments and Quality by Design (QbD) process validations. He presents regularly for ISPE, PDA, AFI, and Sapienza University of Rome. Luca is a trusted expert for cleanroom professionals worldwide.

PMS Logo particle Measuring systems
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.