Inside USP - Pharmaceutical Technology

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Inside USP
  • USP Metals Testing: A Workshop Report


    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


    Pharmaceutical Technology

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

    Inside USP: Metrology and USP Dissolution


    Pharmaceutical Technology

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

    Annual Scientific Meeting Recap


    Pharmaceutical Technology

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

    Revising USP General Notices


    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


    Pharmaceutical Technology

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

    USP's Work Plan and New Revision Approaches


    Pharmaceutical Technology

    Efforts to solicit new monographs have fallen behind the rate of NDA approvals, while analytical techniques have become outdated because of advances in analytical technologies.

    Development of a New USP General Information Chapter: Verification


    Pharmaceutical Technology

    USP's proposed General Chapter 1226 "Verification of Compendial Procedures" aims to provide guidance about the verification process.

    USP Initiatives for the Safe Use of Medical Gases


    Pharmaceutical Technology

    USP monographs, if they are consistently observed and applied, can help reduce medical gas errors.

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