Microbiology,
through regulatory requirements and advances in technology, has become a more
exacting science. This is despite the relatively high variation with many
methods, especially the culture based ones, when compared with analytical
methods designed to recover chemical substances.
In
a new paper, Tim Sandle presents an overview of the validation of
microbiological methods, considering some of the limitations and outlining the
key criteria that may be applicable for assessment.
The
reference is:
Sandle,
T. (2015) Approaching Microbiological Method Validation, Journal of GXP Compliance, 19 (4): 1-15
If
you are interested in viewing a copy, please contact Tim Sandle.
Posted by Dr. Tim Sandle
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