2008年美国药典"The United States Pharmacopeia/National Formulary

书籍目录

The United States Pharmacopeia/National Formulary：Volume 1  Mission Statement and Preface  People    Officers (2005-2010)    Board of Trustees (2005-2010)    Council of Experts (2005-2010)    Council of Experts Executive Committee (2005-2010)    Expert Committees (2005-2010)    Information Expert Committees (2005-2010)    Ad Hoc Advisory Panels (2005-2010)    Members of the United States Pharmacopeial    Convention as of June 1, 2007  Articles of Incorporation..  USP Governance    Constitution and Bylaws    Rules and Procedures    USP Policies  Admissions    Articles Admitted to USP 31 by Supplement    Changes in Official Titles    Revisions Appearing in USP 31 That Were    Not Included in USP 30 Including Supplements    Articles Included in USP 30 but Not    Included in USP 31  Commentary  Notices    USP General Notices and Requirements  General Chapters    See page 29 for detailed contents    General Tests and Assays    General Requirements for Tests and Assays    Apparatus for Tests and Assays    Microbiological Tests    Biological Tests and Assays    Chemical Tests and Assays    Physical Tests and Determinations    General Information    Dietary Supplement  Reagents, Indicators, and Solutions    Reagent Specifications    Indicators and Indicator Test Papers    Chromatographic Reagents    Solutions      Buffer Solutions      Colorimetric Solutions      Test Solutions      Volumetric Solutions  Reference Tables    Containers for Dispensing Capsules and Tablets     Description and Relative Solubility of    USP and NF Articles    Approximate Solubilities of USP and NF Articles    Atomic Weights    Alcoholometric Table    Intrinsic Viscosity Table    Thermometric Equivalents  ……The United States Pharmacopeia/National Formulary：Volume 2The United States Pharmacopeia/National Formulary：Volume 3

作者简介

"The USP-NF" is a single-volume combination of two official compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). Monographs for drug substances and preparations are featured in the USP. Monographs for dietary supplements and ingredients appear in a separate section of the USP. Excipient monographs are included in the NF.The U.S. Federal Food, Drug, and Cosmetics Act designates the USP-NF as the official compendia for drugs marketed in the United States. A drug product in the U.S. market must conform to the standards in USP-NF to avoid possible charges of adulteration and misbranding. The USP-NF is also widely used by manufacturers wishing to market therapeutic products worldwide. Meeting USP-NF standards is accepted globally as assurance of high quality.This title provides six-Month implementation guideline. "United States Pharmacopoeia 31 - National Formulary 26" and its Supplements will become official six months after being released to the public. The USP-NF, which is released on 1 November of each year, will become official on 1 May of the following year. This change was adopted to give users more time to bring their methods and procedures into compliance with new and revised USP-NF requirements.The "United States Pharmacopoeia 31 - National Formulary 26" and any following Supplements and Interim Revision Announcements (IRAs) to that edition, are official as of 1 May 2008, superseding the "United States Pharmacopoeia 30 - National Formulary 25".The CD-ROM edition of the "United States Pharmacopoeia 31 - National Formulary 26" (ISBN 0119899078) is available to buy separately, see below.

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