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Analytics News
News about analytical testing methods in biopharmaceutical manufacturing. Chromatography, UHPLC, chiral. Near-infrared (NIR) and Raman spectroscopy. Anticounterfeiting. Dissolution testing. Cleaning validation. Extracables & leachables.

USP Announces Revision Timeline, Effective Date for Elemental Impurities Limits and Procedures

January 15, 2014

USP announced the approval of General Notices section 5.60.30 Elemental Impurities in USP Drug Products and Dietary Supplements with an official date of Dec. 1, 2015.

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