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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
Junior Advisory Specialist

Irene Maccagli has extensive experience in the pharmaceutical and medical device industries, supporting both quality control and validation departments. Her expertise includes quality assurance and GMP practices, internal inspections for regulatory compliance, developing validation master plans, laboratory method validation, and designing and qualifying cleanrooms. Currently, at PMS, Irene writes documentation to support customers in contamination control strategies for both environmental and utility systems.