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IMMINENT CHANGES TO USP RESIDUAL SOLVENT TESTING-NOT THE USUAL SUSPECTS A major revision to the FDA’s stance on residual solvents testing has been implemented in the U. S. Pharmacopeia (USP) on July 1, 2008. With regard to this, pharmaceutical manufacturers should be aware on the implications of this change, additional testing required and the analytical techniques needed for their manufacturing process. The changing scope of residual solvents testing is discussed on our free technical bulletin which is available for download when you complete the form below. |