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 :
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.
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.
New, legally enforced standards, effective from 1 January 2018. All European Pharmacopoeial texts included.
The British Pharmacopoeia (BP) 2018 supersedes the BP 2017 and becomes legally effective on 1 January 2018. This edition incorporates new BP and European Pharmacopoeia monographs and a significant number of revised monographs.
To ensure you get the best value access to the information you need, there are a range of flexible licences, formats and package options available to choose from.The BP 2018 package
35 new BP monographs, 39 new Ph. Eur. monographs
185 amended BP monographs
Four new monographs for unlicensed formulations
Four new monographs for herbal medicines
A new Supplementary Chapter on Raw materials of Biological Origin for the Production of Cell-based and Gene Therapy Medicinal Products
All European Pharmacopoeia monographs integrated (9th Edition as amended by Supplements 9.1 to 9.2)
Three in-year website and offline download updates to harmonise with the European Pharmacopoeia Supplements 9.3, 9.4 and 9.5
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 StatesHighlights & Features
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
Scientists, professionals, and students working in or with
Flexible access options:
New for 2013:
Your BP 2013 package will include: