USP 40-NF35 2017 FOUR VOLUME SET

Brand: USP
Product Code: USP 40-NF352017 FOUR VOLUME SET
Publishing Date: 2017
Availability: In Stock
Price: Rs73,000.00
Ex Tax: Rs73,000.00
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The USP–NF is a combination of two compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). It contains
standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical  devices, dietary supplements,
and other therapeutics. The current  version of USP–NF standards deemed official by USP are enforceable by the U.S. Food and Drug 
Administration for  medicines manufactured and marketed in the United States. Learn more about the USP–NF and how it is developed. 
A new edition with 2016 standards—USP 40–NF 35—becomes official August 1, 2017.  n official Spanish edition is available in print.

What's Inside USP 40–NF 35
Index
Review and search the combined USP and NF index.
    Admissions List. Find out what's new.
    USP 40–NF 35
    USP 40–NF 35, First Supplement
    Annotated List. Learn what monographs, general chapters, reagents, and tables are affected by changes.
    USP 40–NF 35
    USP 40–NF 35, First Supplement

Features
More than 4,900 monographs with specifications for identity, strength, quality, purity, packaging, and labeling forsubstances and dosage forms
 View a sample USP–NF monograph.
More than 300 general chapters providing clear, step-by-step guidance for assays, tests, and procedures
Focus-specific charts and a combined index help you find the information you need
Helpful sections on reagents, indicators, and solutions, plus reference tables
Includes new General Chapter <800> Hazardous Drugs—Handling in Healthcare Settings

Available Formats

PRINT
Includes a four-volume print main edition and two separate print supplements. Printed on thick, durable paper stock, for laboratory and
manufacturing use. Each volume contains a complete table of contents and index. Shipped with a slipcase for easy access an storage.
Benefits & Applications
The USP–NF offers convenient, comprehensive information for all phases of producing quality prescription, nonprescription, and compounded
medicines excipients; biologics; medical devices; and  dietary supplements. It is essential for quality control, quality assurance, regulatory/
compendia affairs, research and development, method development/analytical services, and corporate management. USP–NF monographs and
methods can help to.

Ensure compliance with required U.S. quality standards
Work to world-recognized standards of precision and accuracy
    Validate test results against proven benchmarks
Establish and validate in-house standard operating procedures, and specifications
Expedite new product development and approvals

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