PMFLIST Archives

July 2020


Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Rodrigo Castillo M <[log in to unmask]>
Reply To:
The Pharmaceutical Microbiology Forum Email List <[log in to unmask]>
Thu, 30 Jul 2020 16:35:19 -0400
text/plain (42 lines)
Dear All,

Im looking guidelines or recommendations that details zones or grade zones in which microbiology operations could be carried out.

The last one that i saw was Annex 2 WHO Good practices in microbiology labs where explain the follow:

Zone Installation                 grade                     Proposed

Sample receipt         Unclassifi ed            Unclassifi ed
Media preparation  Unclassifi ed             Unclassifi ed
Incubator               Unclassifi ed                Unclassifi ed
Enumeration         Unclassifi eda            Unclassifi ed
Decontamination Unclassifi ed              Unclassifi ed

For Suitability test or GPT where we used live microorganims, we need to have a different room or we can used the same that we use for non sterile test? Which guidelines talk about this?

Best regards

The PMFList is supported by our sponsors as a service to the scientific community.

Please take a second to visit our sponsors' web sites and say thank you for their support of this service.
If your company would be interested in sponsoring this community, please contact [log in to unmask]

Steris -

Charles River Laboratories -

Veltek Associates, Inc -

Microbiologics, Inc. -

BD Industrial Media -

Associates of Cape Cod, Inc. -

The nature of this service is to provide a medium for communication.  The specific statements and endorsements of individuals participating in the discussions are not necessarily those of the PMF or the sponsors of the list.