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Zdrowie i gospodarka · 19/10/2007

FDA Releases Draft Guidance on Mechanical Calibration of Dissolution Apparatus for Drug Manufacturers

The Food and Drug Administration (FDA) has made available a draft guidance document to help pharmaceutical companies and testing laboratories use mechanical calibration to calibrate dissolution apparatus, an alternative to calibrator tablets, in order to ensure accurate results in drug testing.

Source: Federal Register — Food and Drug AdministrationOpen original release →