2008年美国药典"The United States Pharmacopeia/National Formulary (Official Compendia of Standards, Vol. 1-3 & 1st & 2nd Supplement) (Paperback)by Council of Experts " 2025 chm pdf kindle rb azw3 下载 115盘

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.

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 2

The United States Pharmacopeia/National Formulary：Volume 3

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书籍介绍

"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.