Management of a Sterile Cleanroom - Pharmaceutical Technology
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Management of a Sterile Cleanroom

There is a risk that consumables' inefficient manufacturing processes may cause contanination of the cleanroom.

This is a particularly important issue if the final product's sterility is dependent upon aseptic processing, rather than sterilising the finished product.

In an aseptic environment, entry of a contaminated consumable product could cause your manufacturing process to fail. It is important to understand the sterilisation methods used by your consumables suppliers and to ensure that their processes have been validated.

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