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Encyclopedia of Biopharmaceutical Statistics

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Shein-Chung Chow, “Encyclopedia of Biopharmaceutical Statistics” ​
Informa HealthCare 2003-06-04 ISBN: 0824742613 1000 pages PDF 57,2 MB​

Millennium Pharmaceuticals, Cambridge, MA. Resource offers more than 3,300 lists expanded to reflect amendments to regulatory requirements and recently developed statistical methods impacting the drug review/approval process and biopharmaceutical research and development. Offers more than 3,000 equations, tables, and figures.
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Fiedler Encyclopedia of Excipients

41FXXJDBZBLtFvyweS.www.arabsbook.com.jpg



Fiedler Encyclopedia of Excipients: For Pharmaceuticals, Cosmetics and Related Areas
Publication Date: 2002-01 ISBN-10 / ASIN: 3871932337 ISBN-13 / EAN: 9783871932335
Binding: Unknown Binding
Publisher: Editio Cantor
Publication Date: 2002-01
ISBN-10 / ASIN: 3871932337
ISBN-13 / EAN: 9783871932335

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المرفقات

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Encyclopedia of Pharmaceutical Technology, Third Edition - 6 Volume Set

By James Swarbrick
Publisher: Informa Healthcare
Number Of Pages: 5536
Publication Date: 2006-10-25
ISBN-10 / ASIN: 084939399X ISBN-13 / EAN: 9780849393990



Presenting authoritative and engaging articles on all aspects of drug development, dosage, manufacturing, and regulation, Encyclopedia of Pharmaceutical Technology, Third edition enables the pharmaceutical specialist to keep abreast of developments in this rapidly evolving and highly competitive field.
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:
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  • 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
Completely new and revised chapters of the Third Edition include:

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  • 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
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التعديل الأخير بواسطة المشرف:
Remington The Science and Practice of Pharmacy 20th Edition

Remington
The Science and Practice
of Pharmacy
20th Edition

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.
A must-have resource for all in the pharmaceutical industry!
Contents
I. Orientation
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  1. Scope of Pharmacy
  2. Evolution of Pharmacy
  3. Ethics and Professionalism
  4. The Practice of Community Pharmacy
  5. Pharmacists in Industry
  6. Pharmacists in Government
  7. Pharmacists and Public Health
  8. Information Resources in Pharmacy and the Pharmaceutical Sciences
  9. Clinical Drug Literature
  10. Research
II. Pharmaceutics
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  1. Metrology and Pharmaceutical Calculations
  2. Statistics
  3. Molecular Structure, Properties, and States of Matter
  4. Complex Formation
  5. Thermodynamics
  6. Solutions and Phase Equilibria
  7. Ionic Solutions and Electrolytic Equilibria
  8. Tonicity, Osmoticity, Osmolality, and Osmolarity
  9. Chemical Kinetics
  10. Interfacial Phenomena
  11. Colloidal Dispersions
  12. Coarse Dispersions
  13. Rheology
III. Pharmaceutical Chemistry
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  1. Inorganic Pharmaceutical Chemistry
  2. Organic Pharmaceutical Chemistry
  3. Natural Products
  4. Drug Nomenclature—United States Adopted Names
  5. Structure-Activity Relationship and Drug Design
  6. Fundamentals of Medical Radionuclides
IV. Pharmaceutical Testing, Analysis and Control
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  1. Analysis of Medicinals
  2. Biological Testing
  3. Clinical Analysis
  4. Chromatography
  5. Instrumental Methods of Analysis
  6. Dissolution
V. Pharmaceutical Manufacturing
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  1. Separation
  2. Powders
  3. Property-Based Drug Design and Preformulation
  4. Solutions, Emulsions, Suspensions and Extracts
  5. Sterilization
  6. Parenteral Preparations
  7. Intravenous Admixtures
  8. Ophthalmic Preparations
  9. Medicated Topicals
  10. Oral Solid Dosage Forms
  11. Coating of Pharmaceutical Dosage Forms
  12. Extended-Release and Targeted Drug-Delivery Systems
  13. The New Drug Approval Process and Clinical Trial Design
  14. Biotechnology and Drugs
  15. Aerosols
  16. Quality Assurance and Control
  17. Stability of Pharmaceutical Products
  18. Bioavailability and Bioequivalency Testing
  19. Plastic Packaging Materials
  20. Pharmaceutical Necessities
VI. Pharmacodynamics
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  1. Diseases: Manifestations and Pathophysiology
  2. Drug Absorption, Action and Disposition
  3. Basic Pharmacokinetics and Pharmacodynamics
  4. Clinical Pharmacokinetics and Pharmacodynamics
  5. Principles of Immunology
  6. Adverse Drug Reactions and Clinical Toxicology
  7. Pharmacogenomics
  8. Pharmacokinetics/Pharmacodynamics in Drug Development
VII. Pharmaceutical and Medicinal Agents
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  1. Diagnostic Drugs and Reagents
  2. Topical Drugs
  3. Gastrointestinal and Liver Drugs
  4. Blood, Fluids, Electrolytes and Hematological Drugs
  5. Cardiovascular Drugs
  6. Respiratory Drugs
  7. Sympathomimetic Drugs
  8. Cholinomimetic Drugs
  9. Adrenergic Antagonists and Adrenergic Neuron Blocking Drugs
  10. Antimuscarinic and Antispasmodic Drugs
  11. Skeletal Muscle Relaxants
  12. Diuretic Drugs
  13. Uterine and Antimigraine Drugs
  14. Hormones and Hormone Antagonists
  15. General Anesthetics
  16. Local Anesthetics
  17. Antianxiety Agents and Hypnotic Drugs
  18. Antiepileptic Drugs
  19. Psychopharmacologic Agents
  20. Analgesic, Antipyretic, and Anti-inflammatory Drugs
  21. Histamine and Antihistaminic Drugs
  22. Central Nervous System Stimulants
  23. Antineoplastic Drugs
  24. Immunoactive Drugs
  25. Parasiticides
  26. Immunizing Agents and Allergenic Extracts
  27. Anti-Infectives
  28. Enzymes
  29. Nutrients and Associated Substances
  30. Pesticides
VIII. Pharmacy Practice
Fundamentals of Pharmacy Administration
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  1. Applications of Ethical Principles to Practice Dilemmas
  2. Technology and Automation
  3. The Patient: Behavioral Determinants
  4. Patient Communication
  5. Patient Compliance
  6. Drug Education
  7. Professional Communications
  8. The Prescription
  9. Providing a Framework for Ensuring Medication Use Safety
  10. Poison Control
  11. Drug Interactions
  12. Extemporaneous Prescription Compounding
  13. Nuclear Pharmacy Practice
  14. Nutrition in Pharmacy Practice
  15. Pharmacoepidemiology
  16. Surgical Supplies
  17. Health Accessories
Social, Behavioral, andEconomic, and Administrative Sciences
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  1. Laws Governing Pharmacy
  2. Re-engineering Pharmacy Practice
  3. Pharmacoeconomics
  4. Community Pharmacy Economics and Management
  5. Product Recalls and Withdrawals
  6. Marketing Pharmaceutical Care Services
  7. Documenting, Billing, and Reimbursement for Pharmaceutical Care Services
  8. Pharmaceutical Risk Management
  9. Integrated Health Care Delivery Systems
Patient Care
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  1. Specialization in Pharmacy Practice
  2. Pharmacists and Disease State Management
  3. Development of a Pharmacy Care Plan and Patient Problem-Solving
  4. Ambulatory Patient Care
  5. Self-Care
  6. Diagnostic Self-Care
  7. Preventive Care
  8. Hospital Pharmacy Practice
  9. Emergency Medicine Pharmacy Practice
  10. Long-Term Care
  11. Aseptic Processing for Home Infusion Pharmaceuticals
  12. The Pharmacist's Role in Substance Use Disorders
  13. Complementary and Alternative Medical Health Care
  14. Chronic Wound Care



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