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Inside USP

Inside USP: Characterization of Heparin Products

October 2, 2009

Pharmaceutical Technology

USP workshop participants support new methods to safeguard heparin products but desire international harmonization. This article contains bonus online-exclusive material.

Traditional Chinese Medicines and Western Regulatory Paradigms

July 2, 2009

Pharmaceutical Technology

Traditional Chinese Medicine is widely used, but questions persist regarding its regulatory status.

Heparin Monographs Further Revised

March 2, 2009

Pharmaceutical Technology

USP's Stage 2 heparin monograph revisions address identification, potency, and impurities.

USP Metals Testing: A Workshop Report

November 2, 2008

Pharmaceutical Technology

Attendees at a recent workshop endorsed new methods to detect metals in drugs, dietary supplements, and food ingredients.

US Pharmacopeia Guideline for Pending Monographs

August 2, 2008

Pharmaceutical Technology

USP's guideline for pending monographs can speed up publication of monograhs and time to market.

Inside USP: Metrology and USP Dissolution

March 2, 2008

Pharmaceutical Technology

The United States Pharmacopeia emphasizes mechanical calibration and a performance test to esnure integrity of the dissolution procedure.

Annual Scientific Meeting Recap

November 2, 2007

Pharmaceutical Technology

Representatives from 17 nations sit down to decide upon standards-setting initiatives.

Revising USP General Notices

August 2, 2007

Pharmaceutical Technology

USP is revising key documents to make them easier to use.

Dissolution Testing and Metrological Measurement of Quality for Solid Oral Dosage Forms

May 2, 2007

Pharmaceutical Technology

USP applies metrological principles to the dissolution procedure alone and in collaborative studies to understand and minimize potential sources of variability.

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