PHARMA BOOKS
>> Sunday, June 19, 2011
John Block, John M Beale, "Wilson & Gisvold's Textbook of Organic Medicinal and Pharmaceutical Chemistry"
Lippincott Williams & Wilkins | 2003 | ISBN: 0781734819 | 1000 pages | PDF (scan) | 213 MB
Lippincott Williams & Wilkins | 2003 | ISBN: 0781734819 | 1000 pages | PDF (scan) | 213 MB
Oregon State Univ., Corvallis. Blends the chemical and pharmaceutical principles necessary for understanding structure-activity relationships and molecular mechanisms of drug action. Offers new information on emerging trends and advances and the challenges posed by new diseases. Features a new chapter on combinatorial chemistry.
Part 1
Part 2
Part 3
British National Formulary for Children 2009
By Paediatric Formulary Committee
Publisher: Pharmaceutical Press 2009 974 Pages ISBN: 0853698473 PDF 6.11 MB
By Paediatric Formulary Committee
Publisher: Pharmaceutical Press 2009 974 Pages ISBN: 0853698473 PDF 6.11 MB
| “ | BNF for Children (BNFC) provides essential practical information to all healthcare professionals involved in the prescribing, dispensing, monitoring and administration of medicines to children. The resource addresses a significant knowledge gap in many areas of paediatric practice by providing practical information on the use of medicines in children of all ages from birth to adolescence. | ” |
The British Pharmacopoeia" ("BP") 2009
Stationery Office Books ISBN: 011322799X 95 MB 3500 pages PDF Rapidshare
Stationery Office Books ISBN: 011322799X 95 MB 3500 pages PDF Rapidshare
Product Description
"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.
Elizabeth Williamson, Samuel Driver, Karen Baxter, "Stockley's Herbal Medicines Interactions"
Pharmaceutical Press 2009 ISBN: 0853697604 400 pages PDF 2,3 MB
Pharmaceutical Press 2009 ISBN: 0853697604 400 pages PDF 2,3 MB
This is a professional level major reference work containing information, in A-Z format, on herb-drug, herb-supplement, herb -food and herb-laboratory test interactions; all of which is data referenced. Commercial herbal medicinal products are increasingly consumed on a regular basis by people in the developed world. Often such products are taken concurrently with conventional medicines, frequently without the knowledge of health care professionals. As more evidence has become available, there has been an increasing awareness of the potential and actual problems of interactions, often dangerous, between conventional medicines and herbal medicines. This proposed new major reference brings together available data on approximately 200 of the most commonly used herbal medicines in highly structured, rigorously scientific monographs. Although our texts on herbal medicines and drug interactions include the major well-known interactions, this text is able to treat the subject in considerably more detail.
Nadia Bukhari, David Kearney, "FASTtrack: Therapeutics"
Pharmaceutical Press 2009 ISBN: 0853697752 200 pages PDF 3,3 MB
Pharmaceutical Press 2009 ISBN: 0853697752 200 pages PDF 3,3 MB
This is a revision guide for students providing bullet points of basic information on therapeutics. "FASTtrack" is a new series of indispensable revision guides created especially. The content of each title focuses on what pharmacy students really need to know in order to pass exams, providing concise, bulleted information, key points, tips and an all-important self-assessment section which includes MCQs, case studies, sample essay questions and worked examples. The "FASTtrack" series provides the ultimate lecture notes and is a must-have for all pharmacy undergraduate students wanting to revise and test themselves for forthcoming exams. A "FASTtrack" website includes MCQs, sample online content and much more.
The book every pharmacy students must own!
Pharmacy Student Survival Guide is a one-of-a-kind roadmap for excelling in pharmacy practice courses. A combination calculations, kinetics, drug information, medical terminology, and laboratory data book all in one, the Guide helps you organize case information, improve problem-solving skills, learn terminology, and impress faculty during rounds.
Pharmacy Student Survival Guide is presented in three sections that span the entire pharmacy curriculum:
Systems and Expectations covering ethics, communication, monitoring drug therapy, and regulatory agencies, Patient Care Tool Box covering medical terminology, pharmacokinetics, laboratory data, and physical assessment, Topics in Pharmacy Practice covering Drug Information and Drug Literature Evaluation, Community/Ambulatory Care, Institutional Pharmacy Practice, Public Health, Reducing Health Disparities Through Domestic and Global Outreach to the Undeserved, Valuable for both introductory and advanced practice course, Pharmacy Student Survival Guide is a book you will turn to throughout your entire pharmacy education.
Pharmacy Student Survival Guide is a one-of-a-kind roadmap for excelling in pharmacy practice courses. A combination calculations, kinetics, drug information, medical terminology, and laboratory data book all in one, the Guide helps you organize case information, improve problem-solving skills, learn terminology, and impress faculty during rounds.
Pharmacy Student Survival Guide is presented in three sections that span the entire pharmacy curriculum:
Systems and Expectations covering ethics, communication, monitoring drug therapy, and regulatory agencies, Patient Care Tool Box covering medical terminology, pharmacokinetics, laboratory data, and physical assessment, Topics in Pharmacy Practice covering Drug Information and Drug Literature Evaluation, Community/Ambulatory Care, Institutional Pharmacy Practice, Public Health, Reducing Health Disparities Through Domestic and Global Outreach to the Undeserved, Valuable for both introductory and advanced practice course, Pharmacy Student Survival Guide is a book you will turn to throughout your entire pharmacy education.
Aamer Safdar, Shirley Ip, "Hospital Pre-registration Pharmacist Training"
Pharmaceutical Press 2009 ISBN: 085369785X 256 pages PDF 1,1 MB
Pharmaceutical Press 2009 ISBN: 085369785X 256 pages PDF 1,1 MB
This is a practical guide for students; an insight into their hospital preregistration training. It is one of the RPS "Tomorrow's Pharmacist" series. The proposed text aims to provide a practical explanation for undergraduates and preregistration trainees on what to expect from a hospital preregistration training programme. The text uses an informal writing style and is based on tips, hints, past experiences and anecdotes from the authors in their roles as preregistration tutors. The experiences are from a district general hospital and a large teaching hospital perspective.
This revised edition assesses the range of non-prescription, over-the-counter medicines that can be recommended for the most frequently encountered minor illnesses. The first edition has been updated to reflect changes in the legal status and availability of products and new opinions on and approaches to treatment. A new section on emergency hormonal contraception is also included. The information is presented in a structured formulary format with products described both generically and by brand name along with supplier details. Each chapter also contains a summary of key points with suggestions regarding the most appropriate products. The book should enable pharmacists, GPs, nurses and other healthcare professionals to make well-informed recommendations and to give patients and customers sound advice on non-prescription medicines.
Gordon E. Appelbe, Joy Wingfield, "Dale and Appelbe's Pharmacy Law and Ethics, 9th Edition"
Pharmaceutical Press 2009 ISBN: 0853698279 553 pages PDF 1,9 MB
Pharmaceutical Press 2009 ISBN: 0853698279 553 pages PDF 1,9 MB
This is a comprehensive guide to law and ethics for pharmacy practice in the UK. "Dale and Appelbe's Pharmacy Law and Ethics" has become established as the standard student textbook and reference work on this subject in the UK. A knowledge of pharmacy law is a substantial and compulsory component of the undergraduate and pre-registration pharmacy syllabus in the UK and changes to the syllabus and practice require the text to be updated regularly. This revised edition provides a comprehensive guide to the law that affects the practice of pharmacy and the use of medicines in Great Britain, and complete coverage of the pharmacy undergraduate and pre-registration syllabus and British law relating to medicines and poisons.
Ram I. Mahato, Sung Wan Kim "Pharmaceutical Perspectives of Nucleic Acid-Based Therapy"
CRC 2002-06-27 ISBN: 041528385X 568 pages PDF 7,3 MB
CRC 2002-06-27 ISBN: 041528385X 568 pages PDF 7,3 MB
Pharmaceutical Perspectives of Nucleic Acid-Based Therapy presents a comprehensive account of gene therapy, from development in the laboratory to clinical applications, with an emphasis on cancer and cardiovascular and autoimmune diseases. Internationally acclaimed scientists discuss the potential use of lipids, peptides and polymers for the in vivo delivery of nucleic acids, the genesis of structure-synthesis-function interrelationships and the evolutionary approaches of these gene carriers. The book also addresses the influence of a viable gene expression system on disease by controlling gene regulation, transcription, translation and replication.
The Merck Index is a one-volume encyclopedia of chemicals, drugs and biologicals that contains more than 10,000 monographs. Each monograph in this authoritative reference source is a concise description of a single substance or a small group of closely related compounds.
Compounds included:
1- human and veterinary drugs
2- biotech drugs and monoclonal antibodie
3- substances used for medical imaging
4- biologicals and natural products
5- plants and traditional medicines
6- nutraceuticals and cosmeceuticals
7- agriculturals, pesticides and herbicides
8- Organic chemicals used in research
9- Food additives and supplements
10- dyes, colors and indicators
11- environmentally significant substances
Information provided:
1- chemical, common and generic names
2- Over 15,000 trademarks and associated companies
3- CAS Registry Numbers for over 12,000 compounds
4- Over 8,500 chemical structures
5- molecular formulae, weights and percentage composition
6- capsule statements identifying compound classes and scientific significance
7- scientific and patent literature references
8- physical and toxicity data
9- therapeutic and commercial uses
10- caution and hazard information
In addition, there are more than 700 new and completely revised monographs, thousands of new references, trademarks and uses added to existing monographs. Now includes a companion CD-ROM which features 989 monographs no longer available in print, organic name reactions, supplemental tables and a new user interface for user-friendly searching.
Features of the CD:
- Searchable by keywords, references, and numerical properties
- Search the complete contents of the 14th edition, plus nearly a thousand monographs archived from previous editions
- Comes with a free one-year subscription to the Merck Index Internet Edition
- Windows-compatible CD powered by CambridgeSoft's ChemFinder
- Extensively revised supplemental tables now including acronyms, vaccines, and physical constants
- More than 70 pages of hard to find information in one easy-to-use place
FREE Download Links: 5 PARTSPart-1
The European Pharmacopoeia is a single reference work for the quality control of medicines in Europe. Several legal texts make the European Pharmacopoeia mandatory:A Convention on the Elaboration of a European Pharmacopoeia ratified in 2003 by 31 European countries and the European Union; European Union directives 2001/83/EC and 2001/82/EC,on medicines for human use and for veterinary use, respectively, maintain the mandatory character of European Pharmacopoeia specifications on medicines as regards their qualitative and quantitative composition and the tests to be carried out on these medicines, the raw materials used in production and the intermediates of synthesis. All producers of medicines or substances for pharmaceutical use therefore must apply the quality standards of the European Pharmacopoeia for the marketing and use of these products in Europe. The texts of the European Pharmacopoeia are legally binding and compliance is enforced by the administrative or juridical authorities. The national authorities of the member states are bound to apply them if necessary replacing any national monograph on the same subject.
The 4th Edition consists of an initial volume 2002 (4.0) and a collection of 8 non-cumulative supplements (4.1) published three times a year following the decisions of each session of the European Pharmacopoeia Commission. With supplement 4.6, the 4th Edition comprises 1750 specific monographs, 285 general methods illustrated by figures or chromatograms and 2140 reagents. Every 4 months a new volume enters into force.
http://rapidshare.com/files/149869347/CDEP4ed.zip
The 4th Edition consists of an initial volume 2002 (4.0) and a collection of 8 non-cumulative supplements (4.1) published three times a year following the decisions of each session of the European Pharmacopoeia Commission. With supplement 4.6, the 4th Edition comprises 1750 specific monographs, 285 general methods illustrated by figures or chromatograms and 2140 reagents. Every 4 months a new volume enters into force.
http://rapidshare.com/files/149869347/CDEP4ed.zip
BioNanotechnology by Elizabeth Papazoglou
Morgan and Claypool Publishers ISBN 1598291386 2007-08-21 PDF 139 Pages 4.6 MB
Morgan and Claypool Publishers ISBN 1598291386 2007-08-21 PDF 139 Pages 4.6 MB
This book aims to provide vital information about the growing field of bionanotechnology for undergraduate and graduate students, as well as working professionals in various fields. The fundamentals of nanotechnology are covered along with several specific bionanotechnology applications, including nanobioimaging and drug delivery which is a growing $100 billions industry. The uniqueness of the field has been brought out with unparalleled lucidity; a balance between important insight into the synthetic methods of preparing stable nano-structures and medical applications driven focus educates and informs the reader on the impact of this emerging field. Critical examination of potential threats followed by a current global outlook completes the discussion. In short, the book takes you through a journey from fundamentals to frontiers of bionanotechnology so that you can understand and make informed decisions on the impact of bionano on your career and business.
CONTENTS
Introduction
0.1 Bionanotechnology: A Historical Perspective
0.2 Nanotechnology and Bionanotechnology
0.3 Notable Nanoimages in Bionanotechnology
0.3.1 AFM-Qd
0.3.2 Nano-drug Delivery Chip
0.3.3 Atomic Force Microscopy Image (AFM) of SWNT
0.3.4 Scanning Electron Microscopy Image (SEM) of SWNT
0.4 Opportunities and Challenges of Bionanotechnology
0.5 Growth potential of Nanotechnology and Related Expenditures
References
1. The Significance of Nano Domain
1.1 Limitations of Micron Size
1.2 Need for Nano-Size—Surface Volume Ratio Significance
1.3 Significance and Key Features of Nano-Size
1.4 Derivation of Bohr’s Atomic Radius of a Hydrogen Atom
1.5 Comparison of Particle Behavior at Nano-Size to Macro Size: Gold and Titania
1.6 Advantages of Scaling Down—Nano-Size
References
2. Nano Drug Delivery
2.1 Conventional Drug Delivery
2.1.1 First Pass Effect
2.1.2 Routes of Delivery
2.2 Targeted Drug Delivery
2.3 Chemistry of Drug Delivery Vehicles
2.3.1 Nanocapsules
2.3.2 Unilamellar Liposomal Vesicles
2.3.3 Nanoparticles
2.3.4 Microemulsions
2.4 Delivery Profiles
2.4.1 Rate-Preprogrammed Drug Delivery Systems
2.4.2 Activation-Modulated Drug Delivery Systems
2.4.3 Feedback-Regulated Drug Delivery Systems
2.4.4 Site-Targeting Drug Delivery Systems
2.5 The Role of Nanotechnology in Drug Delivery
2.5.1 Transdermal
2.5.2 Blood Brain Barrier
2.6 Advantages of Targeted Drug Delivery Systems
References
3. BioNanoimaging
3.1 Quantum Dots
3.2 Ultrasound Contrast Agents
3.3 Magnetic Nanoparticles
References
4. Successful Applications of Bionanotechnology
4.1 Nanostructures and Nanosystems
4.1.1 Nanopore Technology
4.1.2 Nano Self-Assembling Systems
4.1.3 Cantilevers
4.1.4 Nanoarrays
4.2 Nanoparticles
4.2.1 Quantum Dots (QDs)
4.2.2 Paramagnetic Iron Oxide Crystals
4.2.3 Dendrimers
4.2.4 Carbon Nanotubes
4.2.5 Nanosomes and Polymersomes
4.3 In Vitro Diagnostics
4.4 Medical Application of Nanosystems and Nanoparticles
4.4.1 Drug Delivery Applications
4.4.2 Nanoparticles in Molecular Imaging
4.5 Summary and Conclusions
References
5. Synthesis of Gold, Titania, and Zinc Oxide
5.1 Synthesis of Gold
5.1.1 Background
5.1.2 Brust Method of Synthesis of Thiol Derivatized Gold NPs by Biphasic Reduction
5.1.3 Gold Colloids
5.1.4 Gold Nanofilm
5.1.5 Gold Nanorods
5.2 Synthesis of Titania Nanostructures
5.2.1 Background
5.2.2 Solvo-Thermal Synthesis of Titania Nano Crystals
5.2.3 Sol-Gel Template Synthesis of Titania Nano Tubes and Rods
5.2.4 Overview of Other Synthesis Methods
5.3 Synthesis of Zinc Oxide
5.3.1 Background
5.3.2 The Solid-Vapor Synthesis of ZnO
5.1
5.1.1 Brust Method of Synthesis of Thiol Derivatized Gold NPs by Biphasic Reduction
5.2
5.2.1 Solvo-Thermal Synthesis of Titania Nano Crystals
5.2.2 Sol-Gel Template Synthesis of Titania Nano Tubes and Rods
5.2.3 Overview of Other Synthesis Methods
5.3
5.3.1 The Solid-Vapor Synthesis of ZnO: Horizontal Tube Furnace
5.3.2 Wurtzite Structure of ZnO
References
6. Is Bionanotechnology a Panacea?
6.1 Background
6.2 Primary Concerns
6.3 Assessing Potential Risks
6.3.1 Inhalation
6.3.2 Contact/Dermal Delivery
6.3.3 Other Routes of Contact
6.3.4 Environmental Impacts of NPs and the Food Chain
6.3.5 Explosion Hazards
6.4 Lessons from the Past
6.5 Conclusion
References
7. Roadmap to Realization of Bionanotechnology
7.1 Introduction
7.2 Nano Vision: the Futuristic Goals of Bionanotech
7.3 Working toward Realization: Current Progress
7.4 Screenshot of Reality: Bionano-Unbiased/Uncensored
7.5 The Nano Mission: Roadmap to Realization of Translation Research
7.5.1 Bionano in the US
7.5.2 Bio-Nano in Japan
7.5.3 Bio-Nano in UK
7.5.4 UK–Japan Joint Initiative for Bionanotechnology
7.5.5 The EU Initiative in Bionanotech
7.5.6 Bionano in Asia
http://rapidshare.com/files/54677672/BioNanotechnolog.pdf.html
Julius A. Vida - Androgens and Anabolic Agents
Academic Press Inc.,U.S. July 1969 ISBN: 0127218505 328 pages PDF 112 MB
This book is a classic, but you will be very hard up to find it anywhere as it is long out of print. If you have an interest in the science of this topic regardless of whether it is medical or athletic it is a must have. Dr. Vida really put a lot of research and useful explanations in this one. Highly suggested reading.
Alan Nathan, “FASTtrack: Managing Symptoms in the Pharmacy”
Pharmaceutical Press 2007-11-30 ISBN: 0853697272 233 pages PDF 2,05 MB
Pharmaceutical Press 2007-11-30 ISBN: 0853697272 233 pages PDF 2,05 MB
This is a revision guide for students giving bullet points of basic information on managing symptoms in the pharmacy."Fast Track" is a new series of indispensable revision guides created especially for undergraduate pharmacy students.The content of each title focuses on what pharmacy students really need to know in order to pass exams, providing concise, bulleted information, key points, tips and an all-important self-assessment section which includes MCQs, case studies, sample essay questions and worked examples."The Fast Track" series provides the ultimate lecture notes and is a must-have for all pharmacy undergraduate students wanting to revise and test themselves for forthcoming exams.Covering all common ailments, organized by system in alphabetical order, this book provides all the essential information needed for managing symptoms presented in the pharmacy.A Fast Track website will also be live at time of publication and will include MCQs, and samples.
Textbook of Pharmacoepidemiology
Publisher: Wiley Language: English ISBN: 0470029250 518 pages Data: 2007 PDF 3 Mb
Publisher: Wiley Language: English ISBN: 0470029250 518 pages Data: 2007 PDF 3 Mb
Description: The Textbook of Pharmacoepidemiology provides a streamlined text for evaluating the safety and effectiveness of medicines. It includes a brief introduction to pharmacoepidemiology as well as sections on data sources, methodology and applications. Each chapter includes key points, case studies and essential references.
* One-step resource to gain understanding of the subject of pharmacoepidemiology at an affordable price
* Gives a perspective on the subject from academia, pharmaceutical industry and regulatory agencies
* Designed for students with basic knowledge of epidemiology and public health
* Includes many case studies to illustrate pharmacoepidemiology in real clinical setting
Alan Crozier "Plant Secondary Metabolites: Occurrence, Structure and Role in the Human Diet"
Wiley-Blackwell 2006-12-11 ISBN: 1405125098 384 pages PDF 9 MB
Wiley-Blackwell 2006-12-11 ISBN: 1405125098 384 pages PDF 9 MB
Plant Secondary Metabolites: Occurrence, Structure and Role in the Human Diet covers the main groups of natural products from a chemical and biosynthetic perspective with illustrations of how genetic engineering can be applied to manipulate levels of secondary metabolites of economic value as well as those of potential importance in diet and health. These descriptive chapters are augmented by chapters showing where these products are found in the diet, how they are metabolized and reviewing the evidence for their beneficial bioactivity.
Publisher: World Scientific Publishing CompanyNumber Of Pages: 150
Publication Date: 2007-05-29
ISBN-10 / ASIN: 9812706607
ISBN-13 / EAN: 9789812706607
Binding: Paperback
Product Description:
Innovation is at the heart of all advances and has the capacity to solve problems facing humanity. Societies which have turned away from innovation and technological development have failed in their ability to support their populations. Understanding the nature of innovation in the life sciences and in particular healthcare, how it operates, what enables and hinders it is therefore of great importance to meeting the challenges ahead. This book, originally and concurrently published in the International Journal of Innovation Management, Vol. 11, No. 2, 2007, offers the latest research and insights concerning innovation in the biopharmaceutical industry.
http://rapidshare.com/files/12 371040...L_INDUSTRY.pdf
By James Swarbrick
Publisher: Informa Healthcare
Number Of Pages: 5536
Publication Date: 2006-10-25
ISBN-10 / ASIN: 084939399X ISBN-13 / EAN: 9780849393990
A dependable reference tool and constant companion for years to come, the Third Edition offers completely new entries that cover critical issues in the field such as the impact of genomics, biotechnology, and implants on drug discovery, targeting, delivery, and formulation.
In addition, it addresses new regulatory issues, such as the changes in advertising regulations, and emerging FDA procedures.
Bringing together acknowledged leaders from every specialty related to pharmaceutical technology, this Third Edition:
- stands as an indispensable and single-source reference at the forefront of pharmaceutical technology and research
- keeps pharmaceutical professionals and researchers at the cutting-edge of their disciplines with more than 70 NEW entries on topics of utmost importance in the field including advances in systems validation, processing techniques, patent issues, noninvasive drug delivery, and the commercialization of drugs and dosage forms
- provides a comprehensive overview of most specialty and subspecialty topics relating to the research, manufacture, marketing, and use of pharmaceuticals
- offers a reader-friendly and timely collection of references to the pharmaceutical market
- contains an abundance of articles on pharmaceutics, pharmacokinetics, analytical chemistry, quality assurance, drug safety, and manufacturing processes
- 21 CFR Part 11 Revisited
- Adsorption at Solid Surfaces - Pharmaceutical Applications
- Alternative Medicines
- Amorphous Pharmaceutical Systems
- Bioavailability of Drugs and Bioequivalence
- Biotechnology and Biological Preparations
- Biotechnology-Derived Drug Products: Formulation Development
- Biotechnology-Derived Drug Products: Stability Testing, Filling, and Packaging
- Bio-validation of Steam Sterilization
- Buffers, Buffering Agents, and Ionic Equilibria
- Calorimetry in Pharmaceutical Research and Development
- Capsules, Hard
- Capsules, Soft
- Clinical Supplies Manufacture: GMP Considerations
- Cocrystallization
- Cold Chain Distribution of Pharmaceuticals
- Computer Systems Validation
- Continuous Processing of Pharmaceuticals
- Corrosion of Pharmaceutical Equipment
- Crystal Habit Changes and Dosage Form Performance
- Crystallization: Significance on Product Development, Processing, and Performance
- Dendrimers
- Dissolution and Dissolution Testing
- Dressings in Wound Management
- Drug Delivery - Pulsatile Systems
- Drug Delivery across the Blood-Brain Barrier
- Drug Delivery Systems: Neutron Scattering Studies
- Drug Information Systems
- Drug Master Files
- Drug Transporters
- Dry Powder Aerosols, Emerging Technologies
- Electrical Power Systems for Pharmaceutical Equipment
- Electrochemical Detection for Pharmaceutical Analysis
- Electrostatic Charge in Pharmaceutical Systems
- European Agency for the Evaluation of Medicinal Products (EMEA)
- Extractables and Leachables in Drugs and Packaging
- Fast-Dissolve Drug Delivery Systems
- Film Coating of Oral Solid Dosage Forms
- Fine Particle Processing Techniques in Pharmaceutics
- Fluid Bed Processes for Forming Functional Particles
- Forced Degradation Studies
- Formulation Patent Issues
- Fractal Geometry in Pharmaceutical and Biological Applications - A Review
- Freeze Drying, Scale-Up Considerations
- Gastro-Retentive Systems
- Gelatin-Containing Formulations: Changes in Dissolution Characteristics
- Genetic Aspects of Drug Development
- Genetic Materials as Pharmaceuticals
- Handling Hazardous Chemicals and Pharmaceuticals
- Headspace Oxygen Analysis in Pharmaceutical Products
- Hydrogels
- Implantable Biomedical Devices
- IV/IC Correlation
- Laboratory Information Management System (LIMS)
- Liquid Oral Preparations
- Materials of Construction for Pharmaceutical Equipment
- Melt Processes for Oral Solid Dosage Forms
- Metabolite Identification in Drug Discovery
- Microbiologic Monitoring of Controlled Processes
- Microencapsulation Technology
- Milling of Pharmaceuticals
- Molecular and Cellular Approaches to Lead Optimization in Pharmaceutical Development
- Nanoparticle Engineering
- Needle-Free Drug Delivery
- Neural Computing and Formulation Optimization
- Noninvasive Protein and Peptide Delivery
- Nonprescription Drugs
- Nutraceutical Supplements
- Oligonucleotides: Bioanalytical Techniques
- Packaging Systems: Compendial Requirements
- Particle Engineering
- Particle Size Control during Crystallization. Patents - International Perspective
- Peptides and Proteins - Nasal Absorption
- Pharmacogenomics and Genomic Technologies
- Pharmacokinetics: Effects of Food and Fasting
- Pilot Plant Design
- Pilot Plant Operation
- PK/PD Modeling and Simulations in Drug Development
- Polymeric Delivery Systems for Poorly Soluble Drugs
- Polymers in Transdermal Delivery Systems
- Population Pharmacokinetics
- Powder Sampling
- Preformulation Studies on Drugs
- Proteomics, Pharmaceutical Applications
- Quality Assurance of Pharmaceuticals
- Quality Systems Management
- Radiolabelling of Pharmaceutical Aerosols and Gamma Scintigraphic Imaging for Lung Deposition
- Rheology of Pharmaceutical Systems
- RNAi in Drug Development
http://rapidshare.com/files/79551667/Encyclopedia_Pharma_Tech_3Ed.zip
Or
Or
Or
The aim of Therapeutic Guidelines Limited (TGL) is to provide clear, practical, authoritative and succinct therapeutic information for busy health practitioners, for the management of patients with specific conditions.
The recommendations in Therapeutic Guidelines are based on the latest international literature, interpreted by some of Australia’s most eminent and respected experts, with each statement having been examined, subjected to challenge and discussed over a series of day long meetings. The finished texts represent the essence of current available evidence.
The aim of Therapeutic Guidelines Limited (TGL) is to provide clear, practical, authoritative and succinct therapeutic information for busy health practitioners, for the management of patients with specific conditions.
The guidelines are comprehensive in that they cover all common disorders seen in clinical practice. The information is independent and unbiased and is a distillation of current evidence and opinion. The text is arranged into chapters and sections according to diagnostic entities. Each section gives sufficient surrounding information to orient the reader followed by succinct and explicit recommendations for therapy.
The guidelines are not primarily meant to instruct, but rather to assist prescribers in ensuring patients receive optimum treatment.
The content of each title is revised by an expert group every 3 to 4 years. The iterative cycles are based on response to feedback, and shifts in the evidence base.
The essential principles underlying this process for guideline development stem from the production of the first guidelines in 1978, with the method being both refined and improved over the years.
CHM Format
30.98 MB
Download
Or
Http://ifile.it/2qfu9z3
0 comments:
Post a Comment