12 – Microbiological Control for non-sterile pharmaceuticals


Managing microbiological contamination risks associated with non-sterile products is a clear expectation from regulatory agencies. This monograph provides a comprehensive guide on all aspects of microbiological control from facility design to staff training, and from risk assessment to microbiological monitoring. This Monograph was produced jointly by PQG and Pharmig. It was first published in November 2008.


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