Introduction: Why Contamination Control Is the Heart of Cleanroom Design

Cleanrooms are built not for people, but for the products and processes that must remain uncontaminated. Whether it’s a sterile pharmaceutical vial, a semiconductor wafer, or a medical implant, the slightest contamination can compromise safety, quality, and yield.

But contamination doesn’t happen randomly. It has sources, pathways, and mechanisms—all of which can be identified and controlled. This article explores the fundamentals of contamination control, drawing on ISO 14644 standards, GMP Annex 1, and industry best practices.


Part 1: Common Sources of Contamination

Human Operators

Equipment & Materials

Processes

Facility & Air Supply


Part 2: Pathways of Contamination


Part 3: Mitigation Strategies

Engineering Controls

Operational Controls

Validation Controls


Conclusion

Contamination control is a system, not a single solution. By combining engineering, operational, and validation strategies, facilities reduce contamination risk and meet ISO and GMP compliance.

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