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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 "书籍详细信息
- ISBN：9781889788531
- 作者：暂无作者
- 出版社：暂无出版社
- 出版时间：2007-11
- 页数：3788 页
- 价格：1290.00
- 纸张：胶版纸
- 装帧：精装
- 开本：8开
- 语言：未知
- 丛书：暂无丛书
- TAG：暂无
- 豆瓣评分：暂无豆瓣评分
内容简介：
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.
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 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.
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