There
is a vast array of different products on the market. Few are manufactured and
sold specifically for pharmaceuticals; most are developed for the healthcare
sector and sold across both healthcare and pharmaceuticals. Generally, given
the similarity in disinfectant efficacy testing standards, the cross use of
such products is not problematic with the exception that products used in
higher grade pharmaceutical cleanrooms need to be sterile. Although many
products are available, the US Food and Drug Administration (FDA) is concerned
about their effectiveness and the federal agency has opened a review in
relation to healthcare use.
Because
of the cross marketing and limited range of active ingredients in such products,
this review will cut across the pharmaceutical sector. The use of hand disinfectants
embraces a number of GMP concerns.
In
light of this, Tim Sandle has written an article about the review and the
implications for the pharmaceutical sector. The article is published in the GMP
Review.
The
reference is:
Sandle,
T. (2015) FDA opens up review into hand disinfectants, GMP Review, 14 (2): 8-9
Posted by Tim Sandle
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