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Remington: The Science and Practice of Pharmacy

2008-11-14T20:03:00.002+05:30

For over 100 years, Remington has been the definitive textbook and reference on the science and practice of pharmacy. This Twenty-First Edition keeps pace with recent changes in the pharmacy curriculum and professional pharmacy practice. More than 95 new contributors and 5 new section editors provide fresh perspectives on the field. New chapters include pharmacogenomics, application of ethical principles to practice dilemmas, technology and automation, professional communication, medication errors, re-engineering pharmacy practice, management of special risk medicines, specialization in pharmacy practice, disease state management, emergency patient care, and wound care. Purchasers of this textbook are entitled to a new, fully indexed Bonus CD-ROM, affording instant access to the full content of Remington in a convenient and portable format.

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Part - I: http://rapidshare.com/files/45552201/Remington.part1.rar

Part - II: http://rapidshare.com/files/45685773/Remington.part2.rar

Injectable Dispersed Systems: Formulation, Processing and Performance

2008-11-14T19:56:00.002+05:30

This authoritative guide will serve as the most current source on the design and manufacturing of parenteral dispersed systems-showcasing the utility of dispersed systems in drug delivery, drug targeting, and pharmaceutical engineering.

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http://rapidshare.com/files/49491773/Inject_Dispersed_Sys.rar

HPLC Method Development for Pharmaceuticals, Volume 8

2008-11-14T19:52:00.001+05:30

High pressure, or high performance, liquid chromatography (HPLC) is the method of choice for checking purity of new drug candidates, monitoring changes during scale up or revision of synthetic procedures, evaluating new formulations, and running control/assurance of the final drug product. HPLC Method Development for Pharmaceuticals provides an extensive overview of modern HPLC method development that addresses these unique concerns. Includes a review and update of the current state of the art and science of HPLC, including theory, modes of HPLC, column chemistry, retention mechanisms, chiral separations, modern instrumentation (including ultrahigh-pressure systems), and sample preparation. Emphasis has been placed on implementation in a pharmaceutical setting and on providing a practical perspective.

HPLC Method Development for Pharmaceuticals is intended to be particularly useful for both novice and experienced HPLC method development chemists in the pharmaceutical industry and for managers who are seeking to update their knowledge.

* Covers the requirements for HPLC in a pharmaceutical setting including strategies for software and hardware validation to allow for use in a regulated laboratory
* Provides an overview of the pharmaceutical development process (clinical phases, chemical and pharmaceutical development activities)
* Discusses how HPLC is used in each phase of pharmaceutical development and how methods are developed to support activities in each phase

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http://rapidshare.com/files/74149161/HPLC_Method_Develop_Pharma.zip

Pharmaceutical Dosage Forms:Disperse systems volume 1

2008-11-14T19:46:00.002+05:30

Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this Second Edition of a well-received reference test highlights typical formulations, the avoidance of formulation pitfalls, and compliance with established regulatory principles.

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http://rapidshare.com/files/78701360/Dispersed_Systems.zip

Advanced Pharmaceutical Solids

2008-11-14T19:44:00.002+05:30

This extensive reference/text explores the principles, instrumentation, processes, and programs of pharmaceutical solid science as well as new aspects on one-component systems, micromeritics, polymorphism, solid-state stability, cohesion, powder flow, blending, single- unit sustained release, and tablet coating. Reveals unique approaches in pharmaceutical solid science not previously published in any other text! Providing current data on crystallization, dissolution from particles and polydisperse populations, powder volumes and densities, comminution, wet granulation, and hard-shell capsules, Advanced Pharmaceutical Solids · describes moisture isotherms with crystalline solids · documents the effects of moisture on solid-state stability · highlights tablet physics and principles · explains sustained release by microencapsulation · presents prediction equations for solubility in binary solvents · discusses particle sizes and diameters · identifies Brunauer, Emmett, and Teller Isotherms · and more! Considering properties of solids, permeamitry and gas absorption methods, amorphates, and purification by pH-change precipitation, Advanced Pharmaceutical Solids is an essential reference for pharmacists; pharmaceutical scientists; medicinal, physical, surface, colloid, and analytical chemists and biochemists; and an effective text for upper-level undergraduate and graduate students in these disciplines.
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http://rapidshare.com/files/69808903/Adv_Pharma_Solid.zip

Generic Drug Formulations

2008-11-14T19:40:00.000+05:30

A selection of about 500 formulations of human and veterinary drugs are presented in this booklet. They have all been developed in the last 20 years in the Applications Laboratories of BASF AG and are in solid, liquid, and semi-solid form. However, emphasis is placed on tablets. Human and veterinary medicines have not been dealt with in separate chapters, because the technologies and excipients are the same.

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http://rapidshare.com/files/62246601/generic.zip

Dermatological and Transdermal Formulations

2008-11-14T19:26:00.003+05:30

Containing 350 illustrations, tables, and equations and covering AAPS/FDA guidelines for the experimentation and analysis of in vivo and in vitro percutaneous absorption, this reference provides comprehensive coverage of the development, preparation, and application of topical and transdermal therapeutic systems. Recognized international experts discuss the bioequivalence of dermatological and transdermal dosage forms. They explore the biochemistry and treatment of skin diseases, the structure and function of the skin, adverse dermal responses to drug formulations, mechanisms of drug transport through barrier membranes, and methods for measuring and modulating percutaneous permeation.

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Rapidshere

MediaMonkey 3.0.6.1190 Final

2008-11-12T12:00:00.000+05:30

MediaMonkey 3.0.6.1190 Final | 7.4Mb

MediaMonkey Gold is the program, intended for the conduct of base of these musical files. This utility allows to collect all musical compositions in a single catalogue. MediaMonkey works with the widespread formats of musical files: MP3, OGG, WMA, MPC, FLAC, APE. She possesses wide possibilities among which it is possible to select followings: support of skinov, built-in CD-ripper, CD-burner and converter audio formats. Also it should be noted such possibility of the program, as aligning the volume of compositions. This function is very useful, for example, at the record of musical disks of format of CDA, when tracks play with a different volume.

Functions of MediaMonkey:
- Copying of tracks from compact disks,
- Record of tracks on CD or DVD,
- Converting of tracks from one format in other.
- Editing of ID3 of tegov files.
- Automatic filling of tegov from the text of the name of file or
from the Internet.
- Creation of pleylistov.
- Groupment of compositions on the parameters of tegov in a
musical manager.
- Adjusting of volume of the lost tracks.
- Changeable themes of visual registration.
- And great deal, other great deal...

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Adobe CS4 Production Premium Multilanguage Retail ISO

2008-11-12T11:54:00.000+05:30

Adobe CS4 Production Premium Multilanguage Retail ISO

Adobe CS4 Production Premium Multilanguage Retail ISO CD/DVD | 12 GB

Adobe Creative Suite 4 Production Premium software is a must-have solution for creative professionals who need to craft world-class video, audio, and interactive media — on air, online, on device, and invariably on deadline.

CD1: Content
CD2: Learning
4DVD

Inside:
After Effects CS4
Adobe Premiere CS4
Photoshop CS4 Extended
Flash CS4 Professional
Illustrator CS4
Soundbooth CS4
Adobe OnLocation CS4
Encore CS4
Adobe Bridge CS4
Adobe Device Central CS4
Dynamic Link

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Portable Winamp 5.531 Build 1938 Pro Multilanguage

2008-06-03T15:07:00.000+05:30

Portable Winamp 5.531 Build 1938 Pro Multilanguage Size: 11 MB
Nullsoft Winamp is a fast, flexible, high-fidelity media player for Windows. Winamp supports playback of many audio (MP3, OGG, AAC, WAV, MOD, XM, S3M, IT, MIDI, etc) and video types (AVI, ASF, MPEG, NSV), custom appearances called skins (supporting both classic Winamp 1.x/2.x skins and Winamp 3 freeform skins), audio visualization and audio effect plug-ins (including two industry dominating visualization plug-ins), an advanced media library, Internet radio and TV support, CD ripping, and CD burning.

-The Full version plays MP3s, AAC, WMA, and more; Compatible with Winamp 2 Plug-ins; Full Support for classic and modern skins; Plays Videos; has a Powerful Media Library; Browse Internet Radio and TV Stations; Integrated Internet Music Videos and Songs; Bundled Visualizations; and Burn and Rip CDs.-The LITE version plays MP3s, AAC, WMA, and more. It is compatible with Winamp 2 Plug-ins and has full support for classic skins.
Winamp Highlights:-New portable device features - transcoding, new sync options, USB thumbdrive player support, video sync, direct-from-device playback-Faster ripping-Improved AAC and aacPlus encoding-Unicode metadata, filename, and title support-iTunes-compatible gapless playback (MP3/M4A) and encoding (M4A)-Optional 24bit playback-ReplayGain

Link - http://rapidshare.com/files/119521275/winamp.portable.5.531.full.all.rar

Best Games For Nokia Symbian 3rd Edition

2008-05-26T20:49:00.000+05:30

Best Games For Nokia Symbian 3rd Edition

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Microsoft Office 2007 Complete with CD Key

2008-04-25T12:01:00.000+05:30

Portable Microsoft Office 2003 - Word and Excel

2008-04-25T11:52:00.000+05:30

Microsoft Outlook 2003 is a desktop information management program. It only includes Microsoft Word 2003 and Microsoft Excel 2003, no installation required. Now Portable, in your flash drive, only 37 MB.

http://depositfiles.com/en/files/2692219

hsCADCreator 2.0.3.49

2008-03-10T11:42:00.000+05:30

hsCADCreator 2.0.3.49 24,9 MB

This CAD editor allows quick and intuitive design of technical, architectural, and engineering drawings. All the features of leading CAD applications at a fraction of the cost. hsCADCreator is designed to make CAD affordable for individuals, and occasional/novice users, while still providing business users the features they need. es of leading CAD applications at a fraction of the cost. hsCADCreator is designed to make CAD affordable for individuals, and occasional/novice users, while still providing business users the features they need.

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http://rapidshare.com/files/98110400/e-hsc29.rar

CambridgeSoftware ChemOffice Ultra 2008 v11.01

2008-03-10T11:38:00.000+05:30

CambridgeSoftware ChemOffice Ultra 2008 v11.01 380 MBThis ultimate package includes many applications and databases to transforms your PC into a chemical & biological publishing, modeling, and database workstation. ChemOffice is a powerful suite of software, consisting of ChemDraw, Chem3D, ChemFinder and ChemACX for chemists, BioOffice, BioAssay, BioViz, and BioDraw for biologists, and Inventory, E-Notebook and The Merck Index for scientists. ChemOffice and BioOffice are available for micr030ft Windows.

This ultimate chemistry suite includes ChemBioDraw Ultra 11.0, MestReC Std, ChemScript Pro 11.0, ChemBio3D Ultra 11.0, Chem3D interfaces to Schrödinger’s Jaguar and Gaussian, GAMESS Pro 11.0, ChemFinder Ultra 11.0, E-Notebook Ultra 11.0, ChemDraw/Excel and CombiChem/Excel, the ChemDraw and Chem3D ActiveX Pro Plugins & Controls, as well as the ChemINDEX (Index, RXN, NCI & AIDS) databases and a 1-year subscription to ePub. ChemOffice Ultra 2008 adds ChemFinder Ultra, CombiChem/Excel, Chem3D interfaces to Schrödinger’s Jaguar and Gaussian, GAMESS, and a 1-year subscription to ePub to the ChemOffice Pro 2008 suite.
Size : 380 MB

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CambridgeSoftware ChemBioOffice Ultra 2008 v11.01

2008-03-10T11:30:00.000+05:30

ChemBioOffice Ultra is the ultimate chemistry & biology suite designed to meet the needs of both chemists and biologists. ChemBioOffice Ultra 2008 allows scientists to efficiently keep track of their work, gain a deeper understanding of their data, correlate biological activity with chemical structures, and produce scientific reports more professionally and efficiently than ever before.

ChemBioOffice Ultra combines ChemBioDraw Ultra, ChemBio3D Ultra, ChemFinder Ultra, ChemBioViz Ultra, Inventory Ultra, BioAssay Ultra and E-Notebook Ultra in the world’s premier desktop suite designed for both chemists and biologists.

Size : 565 MB

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Japanese Pharmacopoeia

2008-01-28T22:00:00.000+05:30

Number Of Pages: 1357
Publication Date: 2002-01
Sales Rank: 3114417
ISBN / ASIN: 4840806721
EAN: 9784840806725
Binding: Hardcover
Manufacturer: Society of Japanese Pharmac
Studio: Society of Japanese Pharmac

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http://rapidshare.com/files/63351404/Japanese_Pharmacopoeia14.zip

USP NF 2007

2008-01-28T21:17:00.000+05:30

USP NF 2007 (United States Pharmacopeia/National Formulary)

The 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 HERE:

http://rapidshare.com/files/41539644/USP30-NF25.rar

2008-01-28T20:56:00.000+05:30

Avanquest Classic PhoneTools 9.0

2008-01-27T23:45:00.000+05:30

Fax and Phone from your PC Classic PhoneTools is an easy way to turn your PC into a complete communication tool. Our PhoneTools software package provides advanced communication features that easily integrate with your current Windows based system. Classic PhoneTools makes it possible for you to email, fax, telephone and receive voice messages on your PC from a single, efficient interface. This new version of Classic PhoneTools is ideal for professional or personal use and ...

LINK

http://rapidshare.com/files/73494118/Avanquest.Classic.PhoneTools.v9.0.rar

Development and Validation of Analytical Methods (Progress in Pharmaceutical and Biomedical Analysis)

2008-01-27T22:09:00.001+05:30

Development and Validation of Analytical Methods (Progress in Pharmaceutical and Biomedical Analysis)

By C.M. Riley, T.W. Rosanske,

Publisher: Pergamon
Number Of Pages: 362
Publication Date: 1996-05-01
Sales Rank: 1066722
ISBN / ASIN: 0080427928
EAN: 9780080427928
Binding: Hardcover
Manufacturer: Pergamon
Studio: Pergamon
Average Rating: 5

The need to validate an analytical or bioanalytical method is encountered by analysts in the pharmaceutical industry on an almost daily basis, because adequately validated methods are a necessity for approvable regulatory filings. What constitutes a validated method, however, is subject to analyst interpretation because there is no universally accepted industry practice for assay validation. This book is intended to serve as a guide to the analyst in terms of the issues and parameters that must be considered in the development and validation of analytical methods. In addition to the critical issues surrounding method validation, this book also deals with other related factors such as method development, data acquisition, automation, cleaning validation and regulatory considerations.

The book is divided into three parts. Part One, comprising two chapters, looks at some of the basic concepts of method validation. Chapter 1 discusses the general concept of validation and its role in the process of transferring methods from laboratory to laboratory. Chapter 2 looks at some of the critical parameters included in a validation program and the various statistical treatments given to these parameters.

Part Two (Chapters 3, 4 and 5) of the book focuses on the regulatory perspective of analytical validation. Chapter 3 discusses in some detail how validation is treated by various regulatory agencies around the world, including the United States, Canada, the European Community, Australia and Japan. This chapter also discusses the International Conference on Harmonization (ICH) treatment of assay validation. Chapters 4 and 5 cover the issues and various perspectives of the recent United States vs. Barr Laboratories Inc. case involving the retesting of samples.

Part Three (Chapters 6 - 12) covers the development and validation of various analytical components of the pharmaceutical product development process. This part of the book contains specific chapters dedicated to bulk drug substances and finished products, dissolution studies, robotics and automated workstations, biotechnology products, biological samples, analytical methods for cleaning procedures and computer systems and computer-aided validation. Each chapter goes into some detail describing the critical development and related validation considerations for each topic.

This book is not intended to be a practical description of the analytical validation process, but more of a guide to the critical parameters and considerations that must be attended to in a pharmaceutical development program. Despite the existence of numerous guidelines including the recent attempts by the ICH to be implemented in 1998, the practical part of assay validation will always remain, to a certain extent, a matter of the personal preference of the analyst or company. Nevertheless, this book brings together the perspectives of several experts having extensive experience in different capacities in the pharmaceutical industry in an attempt to bring some consistency to analytical method development and validation.

http://rapidshare.com/files/66180590/D___Validation_Ana_Meth.zip