While liquid drugs do not share the compression problems of solid
dosage forms, the filling problems of powder dosage forms, or the
consistency problems of semisolid dosage forms, they do have their
own set of considerations in the formulation and manufacturing
stages. Highlights from Liquid Products, Volume Three include:
practical details involved in complying with the current good
manufacturing practice requirements in liquid manufacturing access
to what an FDA auditor would be looking for during a liquid
manufacturing audit issues that may arise during a US FDA
inspection the protocols used for stability testing for new drugs
and new dosage forms, drawn from the most current ICH guidelines
General
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