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British Pharmacopoeia 2015 (BP 2015)

British Pharmacopoeia 2015 (BP 2015)
  • British Pharmacopoeia 2015 (BP 2015)
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Approx. Price: Rs 88,000 / PieceGet Latest Price


British Pharmacopoeia 2015 (BP 2015)

effective from 1st January 2015

Author: The British Pharmacopoeia Commission Secretariat of the Medicines and Healthcare Products Regulatory Agency (MHRA)
Publisher: TSO (The Stationery Office)

The British Pharmacopoeia (BP) 2015 marks the 150th Anniversary of setting quality standards for medicines and medicinal products in the UK. To celebrate this sesquicentennial year, each copy of the BP 2015 includes a complimentary, commemorative digital facsimile of the BP 1864 – the first edition. This edition also sees the introduction of a USB download format which replaces the CD-ROM.

Updated annually, the BP is the official, authoritative collection of standards for UK medicinal substances for human and veterinary use.

The BP 2015 includes almost 3,500 monographs which are legally enforced by the Human Medicines Regulations 2012, and becomes legally effective on 1 January 2015. Where a pharmacopoeial monograph exists, medicinal products sold or supplied in the UK must comply with the relevant monograph. All monographs and requirements of the European Pharmacopoeia are also reproduced in the BP.

 


Your BP 2015 package will include:

  • A six-volume printed edition, including a single volume of the BP (Veterinary) 2015
  • A single-user USB download key*
  • A single-user license to the online edition*
  • 39 new BP monographs
  • 144 amended monographs
  • One new BP Supplementary Chapter
  • All European Pharmacopoeia monographs integrated (8th Edition as amended by Supplements 8.1 and 8.2)
  • Three in-year updates to harmonise with the European Pharmacopoeia Supplements 8.3 to 8.5
  • USB download format
  • Complimentary 150th Anniversary USB containing a digital facsimile of the BP 1864

 

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The British Pharmacopoeia (BP) 2016 Books

The British Pharmacopoeia (BP) 2016 Books
  • The British Pharmacopoeia (BP) 2016 Books
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Approx. Price: Rs 98,000 / UnitGet Latest Price

Author: The British Pharmacopoeia Commission Secretariat of the Medicines and Healthcare Products Regulatory Agency (MHRA)
Publisher: TSO (The Stationery Office)

The British Pharmacopoeia (BP) 2016 will see the introduction of a new, integrated website pharmacopoeia.com that will provide a single place to access the BP online and to order British Pharmacopoeia Chemical Reference Substances. The site will replace pharmacopoeia.co.uk and will feature more information and a new look with improved functionality and accessibility.

This edition also sees the introduction of a download format for use offline. This replaces the USB, and has the benefit of being updated three times per year to harmonise with the European Pharmacopoeia.

Updated annually, the BP is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products.

The BP 2016 includes almost 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012, and becomes legally effective on 1 January 2016. Where a pharmacopoeial monograph exists, medicinal products sold or supplied in the UK must comply with the relevant monograph. All monographs and requirements of the European Pharmacopoeia are also reproduced in the BP.

 

  • 37 new BP monographs
  • 142 amended monographs
  • One new BP Appendix for the DNA identification of herbs
  • All European Pharmacopoeia monographs integrated (8th Edition as amended by Supplements 8.1 to 8.5)
  • Three in-year updates to harmonise with the European Pharmacopoeia Supplements 8.6 to 8.8
  • Download format
  • Launch of the new pharmacopoeia.com website




  • A six-volume printed edition, including the BP (Veterinary) 2016
  • A single-user download*
  • A single named user licence to BP online*
*These single-user licences are granted solely to the designated holder of the product within an organisation.
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US Pharmacopeia 36 NF 31 Books

US Pharmacopeia 36 NF 31 Books
  • US Pharmacopeia 36 NF 31 Books
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Approx. Price: Rs 70,688 / PieceGet Latest Price
The US Pharmacopeia 36 NF 31 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 4,600 monographs with specifications for identity, strength, quality, purity, packaging, and labeling for substances and dosage forms.
  • More than 260 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:

  • The latest edition, USP 36–NF 31, published on November 1, 2012 in English, and becomes official May 1, 2013. It is available as a one-year subscription in print


Print:


  • Includes a 3-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 in a convenient slipcase for easy access and storage.

 

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:

  • 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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US Pharmacopeia 37 NF 32

US Pharmacopeia 37 NF 32
  • US Pharmacopeia 37 NF 32
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Approx. Price: Rs 70,688 / PieceGet Latest Price

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, online, and USB flash drive 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 and storage.
    • USB Flash Drive The USB flash drive format provides the same quality content found in print, along with viewable chemical structures for more than 700 impurities; FAQs; and quick search, bookmarking, printing, and copy/paste functions. Each main edition and supplement integrates content from all previous editions. Subscribers will receive updates that occur during their subscription period on a new cumulative USB flash drive.
  • All formats feature new, streamlined monograph design for new and revised monographs since USP 33–NF 28 Reissue. The new design is being phased into the compendia in stages.

 

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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