Reducing FDA Form 483 Risks with Modular Cleanrooms

Published on Cell & Gene

Facility design plays a major role in compliance. This article discusses how modular cleanrooms can help reduce the risk of FDA Form 483 violations by improving environmental control, flexibility, and documentation readiness, especially in GMP-regulated environments.

Read the full article on Cell & Gene:

👉 Utilize Modular Cleanrooms to Reduce Your Risk of a Form 483 Violation

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