DETAILS
ISBN: 8190065831
Place of Publication: New Delhi
Publisher: The Controller of Publications
Edition: 1st ed.
Year of Publication: 2003
Physical Description: 140p.
Language: English

SYNOPSIS
The latest edition of the Indian Pharmacopoeia was published in 1996. It was updated by additions and amendments introduced through addendum 2000. Under the Drugs and Cosmetics Act, 1940, the Indian Pharmacopoeia is the legally recognised book of standards for the quality of drug substances and their preparations included therein. In view of the rapid developments is pharmaceutical sciences and technology, it became necessary to make further changes in the existing compendium. Addendum 2002 amends as well as adds new drugs and preparations to the Indian pharmacopoeia 1996 with a view to keeping the pharmacopoeia updated to the extent possible. Besides amending the existing monographs and appendices, it contains 19 new monographs including monographs of 12 antiretroviral drugs and 7 formulations of these substances. A new appendix on residual solvents has been incorporated. Some monographs have undergone major amendments. The appendix on high performance liquid chromatography has been replaced with a new version which also includes the ion chromatography. The Addendum 2002 is a companion volume to the Indian pharmacopoeia which is indispensable for all concerned with the quality of drugs.

DOWNLOAD PART – I

DOWNLOAD PART – II

DOWNLOAD PART – III

Password of RAR File is : www.w5awarez.com

“The British Pharmacopoeia” (”BP”) 2009 is the authoritative, current collection of standards for UK medicinal substances and the official source of all UK pharmaceutical quality standards. It is an essential reference for anyone involved in pharmaceutical research, development, manufacture and testing, and plays a vital role in ensuring that all medicinal substances on the UK market meet standards of safety, quality and efficacy.The “BP” comprises monographs, which set out the mandatory standards for active substances, excipients and formulated preparations, together with supporting General Notices, Appendices (test methods, reagents, etc) and Reference Spectra. Detailed information and guidance on various aspects of current pharmacopoeial policy and practice are provided in the Supplementary Chapters of the “BP”.The “BP” is supplied in a variety of formats designed for ease of use and a wide range of applications. The hard copy edition comprises a five-volume boxed set containing the “BP” in four volumes and the “BP” (Veterinary) volume, plus single user access to the “BP” Online, the dedicated BP website. The online format is easy to network, allowing access for a specified number of users or across an entire organisation site.Following registration – using the ID code supplied with the hard copy – customers will be granted a single user licence to access BP on-line and will have the option to receive the CD-ROM, which contains the whole of the current “British Pharmacopoeia”.It is effective as of 1 January 2009. It includes: a significant number of new UK monographs; all “European Pharmacopoeia 6th Edition” material up to and including “Supplement 6.2″ integrated into the text of “BP 2009″; new and revised monographs for Complementary, Herbal and Homoeopathic medicines with their own section in Volume III; and networking with full technical support from TSO, the publisher of the “BP”. The on-line version delivers the complete text of the “British Pharmacopoeia and European Pharmacopoeia” standards to your PC. The new features include an alphabetical index, user-friendly search interface design, and a facility to create a ‘My BP’ section.” British Pharmacopoeia 2009″ eBook – “The complete British Pharmacopoeia 2009″ is now available exclusively to “BP 2009″ purchasers in an innovative new format. The eBook is greatly suited to this large reference text making the information contained within it available to all of those who wish to access it on the move and away from their desks.British Pharmacopoeia 2009 Concurrent Licence (Online) – “The British Pharmacopoeia” is available as a network licence which can be used on a concurrent user basis. It allows a designated number of staff simultaneous access to the online version of the “British Pharmacopoeia 2009″. Once set up, your workforce can then start using the BP at their convenience.

Key features for the fifth edition include:

• fully updated monographs and references
• 20 full monographs for diseases more commonly seen in the tropics
• invaluable information on dose sizes and administration for babies
• further inclusion of evidence from relevant RCTs and systematic reviews from the Cochrane database
• a free access website with regular updates and links to other useful information.

Download the book:

http://rapidshare.com/files/135459403/tneonatal_formulary.zip

What is the USP–NF?

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.

Monographs and General Chapters

The USP–NF is a three volume 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.

A monograph includes the name of the ingredient or preparation; the definition; packaging, storage, and labeling requirements; and the specification. The specification consists of a series of tests, procedures for the tests, and acceptance criteria. These tests and procedures require the use of official USP Reference Standards. Medicinal ingredients and products will have the stipulated strength, quality, and purity if they conform to the requirements of the monograph and relevant general chapters.

Download:

http://rapidshare.com/files/206124509/USP_30.rar

Presents an historical account of the Pharmacopoeia and describes methods and procedures for the quality control of pharmaceutical substances and dosage forms, including a special section on quality control of anti-malarials.
Free download the book

US Pharmacopeial, ?USP NF 2007 (United States Pharmacopeia/National Formulary)?ISBN 1889788473 1 Har/Pap/ edition (May 2007) CHM 47 MbThe United States Pharmacopeia is a compendium of quality control tests for drugs and excipients to be introduced into a medicinal formulation. It is published every year [1] by the United States Pharmacopoeial Convention. It forms the basis of enforcement actions by the U.S. Food and Drug Administration and the U.S. Drug Enforcement Administration and is the official pharmacopoeia of the U.S.A. and many other nations. Therefore, in case of a dispute, those methods for, amongst others, identification, assay and purity determination of a drug substance or excipient which are stated in the USP will be the legally binding ones.Within the field the compendium is referred to simply as the USP. The initials USP are affixed to materials’ names to indicate that they conform to the specifications in the USP and may be used medicinally.

Download from following link

http://rapidshare.com/files/29017501/American.Pharmacopeia.2007.USP30-NF25.rar__313144e__via_gigapedia.info__.html

http://hideref.com/url/?http://rapidshare.com/files/29017501/American.Pharmacopeia.2007.USP30-NF25.rar

http://www.megaupload.com/?d=2590AG2O

The British Pharmacopoeia (BP) 2007 is the authoritative, current collection of standards for UK medicinal substances and the official source of all UK quality standards. It is an essential reference for anyone involved in pharmaceutical Research & Development, manufacturing and testing, and plays a vital role in ensuring that all medicinal substances on the UK market meet standards of safety, quality and efficacy.

The BP is supplied in a variety of formats designed for ease of use and a wide range of applications. The hard copy edition package contains a boxed five volume set with a separate Veterinary volume, a CD-ROM and access to a comprehensible, regularly updated website. Both the CD-ROM and online formats are easy to network for access across your organisation.

There will not be an edition of the BP entitled ‘British Pharmacopoeia 2006′. In order to improve the alignment of the published edition with the effective date of its contents, the forthcoming edition is entitled ‘British Pharmacopoeia 2007′.

Key features:

• Extensive Revisions including 30 new BP texts
• New Supplementary Chapters containing general guidance on Unlicensed Medicines and Method Validation
• First BP monograph for Traditional Chinese Medicines
• All European Pharmacopoeia 5th edition material up to and including Supplement 5.5 integrated into the text of BP 2007
• Value-for-money networking with full technical support from the publishers
• CD-ROM and website deliver the complete text of the British Pharmacopoeia, British Approved Names and European Pharmacopoeia standards directly to your PC

Free download the book

The sixth edition of The Veterinary Formulary has been updated and revised by 51 expert contributors and reviewed by an advisory committee of veterinarians and pharmacologists. Features of this edition include: Revision of over 780 drug monographs from the fifth edition Some 55 new drug monographs Over 1650 UK veterinary preparations Preparation and dosage details for over 700 human-authorised products Existing sections re-arranged to reflect current veterinary practice Many new sections, eg Prescribing for rabbits, Canine pheromonatherapy, and Teat sealants New table giving husbandry requirements for common pet terrestrial invertebrates Revised BVA code of practice on medicines – includes essential legislation and information New easy-to-read appendix on Drug interactions

Download from following link