Microbiological Environmental Monitoring of Injectable Facility

SUBJECT Microbiological Environmental Monitoring of Injectable Facility 

The procedure and contents described may vary from company to company. The similarity may be noticed due to the nature of the work, which is more or less similar in all companies. The author does not take any responsibility. Each company should validate its own procedure. 

The following are responsible for following the SOP. The quality assurance (QA) manager is responsible for SOP compliance. 

Observe and report any deviation from the proper aseptic techniques in cleanroom. See attachment no. 1700.80(L). 

Document the used sampling techniques and all related details as well as the detected results. 

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