USP 42 - NF37 2019 - United States Pharmacopoeia 42 - National Formulary 37, Publication Date: Nov 1, 2018, print subscription (5 volume set + 2 supplements published in february and june 2019), hardcover edition, english

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 USP 42 - NF37 2019 - United States Pharmacopoeia 42 - National Formulary 37, Publication Date: Nov 1, 2018, print subscription (5 volume set + 2 supplements published in february and june 2019), hardcover edition, english

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O recebimento de encomendas internacionais está sujeito a procedimentos aduaneiros e isto pode causar atrasos além do tempo estimado de entrega. 

 

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USP 42 - N F37 2019 - United States Pharmacopoeia 42 - National Formulary 37, Publication Date: Nov 1, 2018, print subscription (5 volume set + 2 supplements published in february and june 2019), hardcover edition, english

 

The new edition with 2019 standards — USP 42–NF 37 — published in November 2018, and becomes official May 1, 2019.

 

USP–NF Publication Schedule

USP 42–NF 37    
Publication Date: Nov 1, 2018    


First Supplement to USP 42–NF 37
Publication Date: Feb 1, 2019


Second Supplement to USP 42–NF 37    
Publication Date: June 1, 2019

 

Product Details


Format:    Paper
Publisher: United States Pharmacopeial Convention
Publication Date: Nov 1, 2018    
Language: English
Package Dimensions: 12 x 9 x 7.5 inches
ICS    11.120 : Pharmaceutics
Weight(kg.)    10.9450
Year    2019
Country    USA
Keyword    Pharmacopeia


Product Description

 

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.


United States Pharmacopoeia 2019 USP 42–NF 37 – the new edition for 2019 – publishes in English in November 2018. Ensure that you have time to prepare for important standards changes that become official and FDA – enforceable beginning May 1, 2019.

The United States Pharmacopeia–National Formulary (USP–NF) is a book of public pharmacopeial standards. It contains standards for medicines, dosage forms, drug substances, excipients, medical devices, and dietary supplements.

The USP–NF is a 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 in the NF.

Details


The United States Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are developed and relied upon in more than 140 countries.


USP standards are developed and revised by more than 850 volunteer experts, including international participants, who work with USP under strict conflict-of-interest rules. Since its founding in 1820, USP has helped secure the quality of the American drug supply. Building on that legacy, USP today works with scientists, practitioners, and regulators of many nations to help protect public health worldwide.

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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