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Microbiological Monitoring Submissions

If you would like to submit the results of your microbiological monitoring as required under US Pharmacopeia General Chapter 797 (USP 797), you may do so below.

We will accumulate these results and report them to all facilities who submit their data. This will allow facilities in Alaska to benchmark their results with other tribal facilities in the state. The identity of your facility will be kept confidential. We ask for the name of your facility below in order to corroborate the submissions.

Your name :

Your facility :

Date of sampling :

   mm/dd/yy

Incubation time (hrs) :

Incubation temperature (Celsius) :

Type of nutrient agar :

Input your sampling data below. If you do not have data for a specific field, leave it blank. The "Preparation Area" refers to samples taken in areas where the drugs are open to the air, typically inside your biological safety cabinet or laminar airflow workbench. The "Buffer Area" is the zone immediately surrounding your preparation area. The "Ante Area" is the area where you don and doff personal protective equipment and store supplies.

Sample 1

Sample 2

Sample 3

Biological Safety Cabinet

Air Sampling

Surface Sampling (not required)


 

Sample 1

Sample 2

Sample 3

Laminar Airflow Workbench (horizontal flow cabinet)

Air Sampling

Surface Sampling (not required)


 

Sample 1

Sample 2

Sample 3

Buffer Area

Air Sampling

Surface Sampling (not required)


 

Sample 1

Sample 2

Sample 3

Ante Area

Air Sampling

Surface Sampling (not required)