At Microrite, our cleanroom recovery studies demonstrate whether a controlled environment can return to its specified cleanliness level within a defined time after an airborne particulate challenge. This test is highly valuable for verifying the clean-up effectiveness of a cleanroom’s design. Documented in ISO 14644-3:2019 and required by EU GMP Annex 1 for qualification and requalification of non-unidirectional flow cleanrooms, recovery testing is an essential component of regulatory compliance in cGMP manufacturing.

Microrite leverages advanced particle generation, distribution, and counting technologies to perform recovery studies with precision and efficiency. This allows us to deliver high-quality data that not only meets compliance expectations but also provides meaningful insights for operational improvements.

Backed by decades of regulatory expertise, Microrite is trusted worldwide for its science-based approach. Our studies consistently align with ISO and GMP requirements. Each report we produce is audit-ready, complete with detailed analysis and practical recommendations that help our clients strengthen environmental control, reduce risks, and protect product integrity.

With Microrite as your partner, recovery testing becomes more than a regulatory checkbox; it becomes a proactive tool for ensuring compliance, enhancing cleanroom performance, and safeguarding patient safety.