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Contamination Monitoring Blog
april 30, 2020 06:33 AM

Potential Cleanroom Sampling Points per Annex 1 Draft

Written by PMS

In part 4 of our part 5 blog series on Annex 1 Quality Risk Management, we discuss cleanroom sampling points.

Definition of potential sampling points

Sample points include particle counters and microbial monitors.

  • Identification of critical areas by HACCP analysis and process understanding
  • Choose points within the critical areas according to defined criteria
  • When performed this way, you can demonstrate a thorough evaluation based on scientific criteria that any sampling point was considered

Define final cleanroom sampling points based on available space, environmental design, evaluation of product and primary container closure exposure

 

cleanroom sampling points

Contamination Control Advisory Team: Utilities

Our team can help you with your utilities sampling monitoring plan by doing a scientific analysis, through risk-based techniques, of Purified Water, Water for Injection, Pure Steam, and Gases systems for:

  • Points of Use assessment
  • Sampling frequency
  • Sampling procedure
  • Risk mitigation activities

Learn how our Advisory Services Team can help you identify cleanroom sampling points.

Instruments to consider are the Airnet or IsoAir 310P particle sensors, or the Lasair III particle counters. For microbial monitoring you can consider options such as the BioCapt Single Use microbial impactor.

In the next blog in this series we will continue to examine Annex 1 and Quality Risk Management principles and areas where those are discussed.

Want to read more? Jump to other released posts in this series:

  • Part 1 of 5, April 23: Quality Risk Management- Principle Section 2
  • Part 2 of 5, April 24 Quality Risk Management- Annex 1 section 6.1
  • Part 3 of 5, April 28 V/NV Environmental and Process Monitoring- Annex 1, Section 9.4
  • Part 4 of ,5 publishing April 30 Definition of potential sampling points (you are here!)
  • Part 5 of 5, publishing May 1; Blog 5 Process Risk Assessment

 See links to additional supporting resources below: 

  • Paper: Choosing the Most Suitable Particle Sample Point Locations in the Cleanroom
  • On-Demand Webinar: Case Study: Developing an Isolator Filling Line using a Quality Risk Management Approach
  • Blog series: How to Achieve Quality by Design (QbD) in a new Pharmaceutical Fill Line: Intro and Regulatory (Series Part 1 of 6)

Don’t miss an episode of this series. Register for updates on the right column of this page. Click here to contact our Experts for questions.

Filed Under: Advisory, Quality Risk Management, Sampling Points Tagged With: advisory annex 1, cleanroom, filling line, gmp, qrm, sample points, sampling points

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2670 Greve, Denmark

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[email protected]

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