Pharmacopeia Books

British Pharmacopoeia 2013

Approx Price: Rs 70,688 / Piece(s) 
The British Pharmacopoeia (BP) 2013 is the leading collection of standards for UK medicinal products and pharmaceutical substances. Produced by the British Pharmacopoeia Commission Secretariat of the Medicines and Healthcare products Regulatory Agency, the BP makes an important contribution to public health by setting publicly available standards for the quality of medicines.

Features:

 

  • High quality
  • Excellent finishing
  • Good print


Global standards:

 

  • Now used in over 100 countries, the BP remains an essential reference for all individuals and organisations working within pharmaceutical research and development, manufacture and testing around the globe.


Flexible access options:


 

  • The BP 2013 package comprises five volumes of the British Pharmacopoeia 2013 and a single volume of the British Pharmacopoeia (Veterinary) 2013, along with a fully searchable CD-ROM and online access to provide you with flexible resources


New for 2013:

  • Legally effective from 1 January 2013
  • 41 new BP monographs
  • 40 new European Pharmacopoeia monographs
  • 619 amended monographs
  • 6 new and 1 amended Infrared Reference Spectra
  • European Pharmacopoeia 7th edition material up to and including Supplement 7.5
  • Free in-year updates in January, April and July to harmonise with the European Pharmacopoeia

 

Your BP 2013 package will include:

  • Six-volume printed edition including the BP (Veterinary) 2013
  • Single-user licence to the CD-ROM

 

 


 



     

     

    Pharmacopoeia Books of The Peoples Republic of China

    Approx Price: Rs 72,000 / Piece(s) 
    This edition of the Pharmacopoeia of the People’s Republic of China ( known as Chinese Pharmacopoeia 2010 or in abbreviation as ChP 2010 ) has been prepared in accordance with the principles and requirements recommended by the Ninth Pharmacopoeia Commission and accomplished with the effort made by Commission members and its Secretariat and with collaborated support of relevant institutions and organizations. The draft text has been reviewed and approved by the Executive Committee of the Pharmacopoeia Commission. This is the ninth edition of Chinese Pharmacopoeia since the founding of the People’s Republic of China.

    Chinese Pharmacopoeia 2010 is published in three volumes, and contains up to 4567 monographs with 1386 new admissions. In Volume I, it contains monographs of Chinese crude drugs and the prepared slices. Vegetable oil/fat and its extract, the patented Chinese traditional medicines, single ingredient of Chinese crude drug preparations etc. it has 2165 monographs with 1019 new admissions (439 articles of the prepared slice) and 634 revised; Volume II deals with monographs of chemical drugs, , biochemical preparations, radiopharmaceuticals and excipients for pharmaceutical use, contains 2271 monographs with 330 new admissions and 1500 revised; Volume III contains biological products, has 131 monographs with 37 new admissions and 94 revised.

    The number of articles in Appendices of this edition is much varied. There are 14 new admissions and 47 revised, in Volume I. There are 15 new admissions and 69 revised in Appendices of Volume II. There are 18 new admissions and 39 revised in Appendices of Volume III. Appropriate monographs common to all three volumes are presented in each volume respectively in a harmonized and unified form.

    The main changes in the revision of this edition of Chinese Pharmacopoeia are as follows:


    • Monographs adopted in this edition of Chinese Pharmacopoeia are significantly increased comparing with previous editions
    • Applications of contemporary techniques of analysis is further enhanced and stressed in this edition
    • The guarantee of pharmaceutical safety is further strengthened
    • The controllability and effectiveness of drug quality are further improved
    • The contents of drug standards are scientific and normative
    • Encouraging technical innovation, actively participating in international coordinatioin

    US Pharmacopeia 37 NF 32

    Approx Price: Rs 70,688 / Piece 

    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

    International Pharmaceutical and Cosmetics Marketing

    Approx Price: Rs 395 / Piece(s) 
    National and International Pharmaceuticals and Cosmetics Marketing

    by Ranjan Magazine

     

    274 Pages,

    2014 Ed.

    Paperback

     

     

    It s an Important Book on Pharmaceutical and cosmetics marketing for the use od Students, Pharmacists,formulators and Personnel in the marketing sector of the pharmaceutical and cosmetics industry.

     

    The Text Covers all aspects of pharmaceutical and cosmetics marketing like :
    • Nine Right ways to win customers
    • Eleven right ways to increase sales
    • One right way to win arguments
    • Case study of product positioning and stages of product life cycle
    • Right analysis of quality and quantity
    • How the industry can increase business , brand marketing, generic marketing, sales record,etc. and
    • The Vital role of Drugs and Cosmetics Act and rules to avoid Criminal Activities.

     

    This Book aims to help and guide the organisations increase their business which in turn will increase the profits. The Book adequately covers marketing/sales section, laboratory testing section, advertisement section, pictures of pharmaceutical and cosmetics products and price list. All the pharmaceutical and cosmetics products are fundamentally based on synergistic formulations which have been explained; The synergistic effect is greater than the additive effect and is stronger in maintaining better health.

     

    Contents  :

    1. Pharmaceutical and Cosmetics Marketing
    2. Fundamental principles of Marketing Formula
    3. Nine Right ways to win Consumers
    4. One Right way to win Argument
    5. Eleven right ways to increase Sales
    6. Fundamental principles of Calculating and Forecasting Sales Target
    7. Fundamental Principles of Marketing Strategies to Product Positioning, Stages of Product Life Cycle
    8. Right Analysis of Quality and Quantity
    9. Analysis of Right time, Right efforts and Right Money
    10. Fundamental Principles of Administration to Company Organisation to increase Business
    11. Right ways to Consumer needs Satisfaction
    12. Right ways to Brand Marketing
    13. Right ways to generic Marketing
    14. World sales Data
    15. Sales Record
    16. Role of Drugs and Cosmetics Acts and Rules
    17. Cosmetics and Drugs cases
    18. Drugs and Cosmetics Abuse

    INDEX

     

    About Author :

     

    Ranjan Magazine, is currently Plant Head- Manufacturing and Marketing, Sunny Allied Industries, Jammu, J&K. He has authored Books Drugs and Cosmetics Formulationsand Drugs and Cosmetics Act,1940 and Rules,1945.

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