Cleanroom Editorial and News
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Contamination Control Strategies: Comparing Cleanrooms, RABS, Isolators
10/20/2025
Sterile manufacturing relies on three main contamination control strategies (CCSs): cleanrooms, RABS, and isolators. Understand how each system compares in sterility assurance, startup cost, and operational flexibility.
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Applying Appropriate Limits In Cleanroom Monitoring
6/18/2024
Explore ISO 14644-1:2015 and EU GMP Annex 1 in-depth, and learn about cleanroom classification, how to apply monitoring limits in cleanroom environments, and more.
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2024 Emerging Trends In Cleanroom Technologies
8/14/2024
This article shares new market research on pharma/biotech cleanroom technologies, including regional trends, prominent vendors in the space, and more.
- The Critical Role Of Drug Manufacturing Cleanrooms In Controlling Environmental Variables 7/17/2024
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How Particle Counting Efficiency Affects Distribution Data
6/24/2025
Examine how counting efficiency and resolution impact data interpretation in critical environments like cleanrooms and pharmaceuticals.
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When Clean Is The Key To Precision
10/30/2025
Cleanroom micro molding ensures ultra-small components meet strict contamination and performance standards. As devices shrink and precision rises, controlled environments are essential for quality, reliability, and regulatory success.
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5 Key Principles Of Cleanroom Particle Counting
6/24/2025
Discover the five essential principles of cleanroom particle counting and how they ensure compliance, prevent contamination, and protect product quality in highly regulated manufacturing environments.
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What Is OPC Counting Efficiency?
6/24/2025
Ensure cleanroom air quality with optical particle counters. Explore how OPCs work, their performance metrics, and key considerations for choosing the right one.
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ISO Cleanroom Standards
6/24/2025
Explore how ISO 14644 and EU GMP Annex 1 shape cleanroom standards, with a focus on particle control, system accuracy, and the surprising impact of tubing length limitations.
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What To Expect From A Sterile Injectables CDMO
1/20/2026
Sterile injectable manufacturing demands built‑in contamination control, rigorous monitoring, skilled personnel, and robust quality systems, far beyond sterility testing, to ensure safety, compliance, and reliable CDMO performance.