Articles by Tina S. Morris - Pharmaceutical Technology

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Articles by Tina S. Morris

USP Further Strengthens Quality Standards for Heparin

USP optimizes identification tests and impurities procedures.
Sep 2, 2012

USP optimizes identification tests and impurities procedures.

Inside USP: International Dialogue on Biologics Standards

USP promotes horizontal standards for biologics' quality attributes.
Aug 2, 2011

USP promotes horizontal standards for biologics' quality attributes.

Inside USP: Characterization of Heparin Products

USP workshop participants support new methods to safeguard heparin products but desire international harmonization. This article contains bonus online-exclusive material.
Oct 2, 2009

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

Inside USP: Heparin Monographs Further Revised

USP's Stage 2 heparin monograph revisions address identification, potency, and impurities.
Mar 2, 2009

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

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FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
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View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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