US PHARMACOPEIA 37 NF 32 (2014) - 4 Volumes Set + 2 Supplements

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US PHARMACOPEIA 37 NF 32 - 4 Volumes Set + 2 Supplements

effective 1st MAY , 2014

 

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 and storage.

 

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. 

 

Highlights & Features

  • More than 4,700 monographs with specifications for identity, strength, quality, purity, packaging, and labeling for substances and dosage forms. 
  • More than 270 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

Subscription Information

  • A new edition with 2014 standards—USP 37–NF 32—published on November 1, 2013 in English, and becomes official May 1, 2014. It is available as a one-year subscription in print

 

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/compendial 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

A Valuable Reference for

Scientists, professionals, and students working in or with

  • Pharmaceuticals—prescription and nonprescription drugs
  • Biological and biotechnology products
  • Blood and blood products
  • Compounded preparations
  • Cosmetics
  • Dietary supplements
  • Excipients/other drug ingredients
  • Medical devices
  • Medical gases
  • Medical libraries
  • Pharmacies
  • Schools of medicine and pharmacy
  • Veterinary drugs

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