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British Pharmacopoeia (BP) 2020 Six-Volume Printed Edition And Online Access Licence

British Pharmacopoeia (BP) 2020 Six-Volume Printed Edition And Online Access Licence
  • British Pharmacopoeia (BP) 2020 Six-Volume Printed Edition And Online Access Licence
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Approx. Price: Rs 88,000 / SetGet Latest Price

Product Details:

Minimum Order Quantity1 Set
Name Of BookBritish Pharmacopoeia (BP) 2020
AuthorMHRA
Edition2020
BrandMHRA
ColorRed
StandardBritish
Year2020
Binding TypeHardbound
Packaging TypeCarton

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

New, legally enforced standards, available from 1 August 2019. All European Pharmacopoeia texts included.

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

It includes approximately 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a BP monograph exists, medicinal products or active pharmaceutical ingredients sold or supplied in the UK must comply with the relevant monograph.

All monographs and requirements of the European Pharmacopoeia (Ph. Eur.) are reproduced in the BP, making the BP a convenient and fully comprehensive set of standards that can be used across Europe and beyond.

New for the BP 2020

The BP 2020 supersedes the BP 2019 and becomes legally effective on 1 January 2020. This edition incorporates new monographs from both the BP and Ph. Eur. along with a significant number of revised monographs.

  • 35 new BP monographs, 40 new Ph. Eur. monographs
  • 331 amended BP monographs
  • All monographs from the Ph. Eur. 9th Edition and Supplements 9.1 to 9.8 included
  • Ph. Eur. 10th edition, plus supplements 10.1 and 10.2 included as in-year online and download product updates
  • New Timeline Functionality (opens in new window) and cleaner design helps you find the information you need more effectively. Easily see updates, withdrawals and omissions of monographs. Archive subscribers can now identify all previous editions of BP and Ph. Eur., through the improved navigation.
  • We're releasing 16 new BPCRS to coincide with the new and revised monographs in the BP 2020. This means that you can order the new chemical reference standards alongside the BP 2020 - helping you comply with the new standards by January 2020.
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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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