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On Demand | Duration: Aprox. 60 min

Compressed Gas Risk Assessment webinar now on demand

How many companies really have their process gases under control? Can the inadequate or unjustified frequency of monitoring of compressed gas utilities have an impact on the quality of the final products? In paragraph 6.3, the EU GMP Annex 1 states: “Utilities should be designed, installed, qualified, operated, maintained and monitored in a manner to ensure that the utility system functions as expected”. Practical improvement can start with important equipment characteristics, but a strategic investment in the Contamination Control Strategy is also required.

In this webinar, we will show how having a holistic understanding of the utility system and how it integrates with the process is the only way an assessment can be issued to evaluate the final risk that the system may have on the product and its quality.

By attending this webinar, you will gain valuable insights to:

  • Minimize risks associated with compressed gas impurities,
  • Ensure compliance with EU GMP regulations,
  • Improve product quality and consistency.

Register now and take control of your compressed gas systems!

What you'll learn:
  • The critical link between compressed gas quality and final product quality,
  • Regulations and best practices for compressed gas monitoring,
  • Practical tools and strategies for effective control,
  • Defining monitoring frequency and limits based on risk assessment.
Who should attend:
  • Quality assurance
  • Quality control
  • Production and project managers
  • Engineers
  • Facility managers
  • Purchasing and procurement specialists
  • Operations managers
  • Compliance specialists
  • Environmental monitoring specialists
Webinar Presented By:
Irene Maccagli
Contamination Control Advisory Specialist

Irene Maccagli is a recognized expert in pharmaceutical contamination control and GMP-compliant cleanroom operations. With a strong background in quality assurance, laboratory validation, and cleanroom qualification, she has supported quality control and validation departments across the pharmaceutical and medical device industries. Irene specializes in regulatory compliance, internal audits, validation master planning, and laboratory method validation. At Particle Measuring Systems, she develops technical documentation and educational resources to help global manufacturers implement effective environmental monitoring and utility contamination control strategies. Her work supports data integrity, regulatory readiness, and contamination risk reduction in GMP-regulated cleanrooms.

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