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  • Modulation of drug release from hydrophilic matrices
  • Unit Dose Packaging and the U.S. Pharmaceutical Market
  • Analytical Accessories for Formulation and Process Development in Freeze-Drying
  • Disintegration Testing:Strategy for Quality Control Testing of Immediate Release Dosage Forms in Exploratory Development
  • Joint Position Paper on Pharmaceutical Excipient Testing and Control Strategies
  • IPEC's New Safety Evaluation Procedure:A Q&A with IPEC Chairman Dave Schoneker
  • Influence of Superdisintegrants on the Rate of Drug Dissolution from Oral Solid Dosage Forms
  • Functionality-Related Characteristics of Excipients
  • Functionality testing of a multifuntional directly compressible adjuvant containing lactose,pvp and croscarmellose sodium
  • Functionality Comparison of 3 Classes of Superdisintegrants in Promoting Aspirin Tablet Disintegration and Dissolution
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