Daftar e-Book Bidang Ilmu Farmasi

Advances in Biochemical Engineering / Biotechnology

Bidang Ilmu : Farmasi

Penulis : T. Scheper

Abstrak :

This Book is About Advances in Biochemical Engineering / Biotechnology.

Pharmaceutics The Science of Dosage Form Design

Bidang Ilmu : Farmasi

Penulis : M. E. Aulton

Abstrak :

This Book is About Pharmaceutics The Science of Dosage Form Design.

Pharmaceutical Packaging Handbook

Bidang Ilmu : Farmasi

Penulis : Edward J. Bauer

Abstrak :

This Book is About Introduction to the Pharmaceutical Industry: An Overview, Pharmaceutical Dosage Forms and Their Packaging Requirements, Vaccines and Biologically Produced Pharmaceuticals, Medical Foods, The Regulatory Environment, Pharmaceutical Packaging Materials, Medical Device Packaging, Container Fabrication, Sterilization Technology, Container Closure Systems: Completing All Types of Filled Pharmaceutical Containers, Labels and Labeling, Issues Facing Modern Drug Packaging.

Pharmaceutical Dissolution Testing

Bidang Ilmu : Farmasi

Abstrak :

This book is About Historical Development of Dissolution Testing, Compendial Testing Equipment: Calibration, Qualification, and Sources of Error, Compendial Requirements of Dissolution Testing—European Pharmacopoeia, Japanese Pharmacopoeia, United States Pharmacopeia, The Role of Dissolution Testing in the Regulation of Pharmaceuticals: The FDA Perspective, Gastrointestinal Transit and Drug Absorption, Physiological Parameters Relevant to Dissolution Testing: Hydrodynamic Considerations, Development of Dissolution Tests on the Basis of Gastrointestinal Physiology, Orally Administered Drug Products: Dissolution Data Analysis with a View to In Vitro–In Vivo Correlation, Interpretation of In Vitro–In Vivo Time Profiles in Terms of Extent, Rate, and Shape, Study Design Considerations for IVIVC Studies, Dissolution Method Development with a View to Quality Control, Dissolution Method Development: An Industry Perspective, Design and Qualification of Automated Dissolution Systems, Bioavailability of Ingredients in Dietary Supplements: A Practical Approach to the In Vitro Demonstration of the Availability of Ingredients in Dietary Supplements.

Pharmaceutical Stress Testing Predicting Drug Degradation

Bidang Ilmu : Farmasi

Abstrak :

This Book is About Introduction Stress Testing: A Predictive Tool, Stress Testing: The Chemistry of Drug Degradation, Stress Testing: Analytical Considerations, Stress Testing: Relation to the Development Timeline, Role of ‘‘Mass Balance’’ in Pharmaceutical, Oxidative Susceptibility Testing, Comparative Stress Stability Studies for Rapid Evaluation of Manufacturing Changes or Materials from Multiple Sources, Physical and Chemical Stability Considerations in the Development and Stress Testing of Freeze-Dried Pharmaceuticals, Photostability Stress Testing, The Use of Microcalorimetry in Stress Testing, The Power of Computational Chemistry to Leverage Stress Testing of Pharmaceuticals, Solid-State Excipient Compatibility Testing, Stress Testing: Frequently Asked Questions. 

Pharmaceutical Compounding and Dispensing

Bidang Ilmu : Farmasi

Penulis : John F Marriott

Abstrak :

This Book is About History of compounding, Pharmaceutical forms and their preparation, Pharmaceutical forms and their preparation.

Parenteral Quality Control : Sterility, Pyrogen, Particulate, and Package Integrity Testing Third Edition, Revised and Expanded

Bidang Ilmu : Farmasi

Abstrak :

This Book is About Sterility Testing, Pyrogen Testing, Particulate Matter Testing, Package Integrity Testing.

Oral Drug Absorption Prediction and Assessment

Bidang Ilmu : Farmasi

Abstrak :

This Book is About Gastrointestinal Variables, Membrane Permeability, Solubility and Drug Dissolution, In Vivo–In Vitro Correlations.

Handbook Of Pharmaceutical Manufacturing Formulations Semisolid Products Volume 4

Bidang Ilmu : Farmasi

Penulis : Sarfaraz K. Niazi

Abstrak :

This Book is About Regulatory and Manufacturing Guidance1 : Changes to Approved New Drug Applications or Abbreviated New Drug Applications, Postapproval Changes to Semisolid Drugs, Scale-Up and Postapproval Changes for Nonsterile Semisolid Dosage Forms: Manufacturing Equipmen, Stability Testing of Drug Substances and Drug Products, Guidelines for Evaluation of Stability Data in Retest Periods, Skin Irritation and Sensitization Testing of Generic Transdermal Drug Products, Photosafety Testing, Guidance on Formulating Semisolid Drugs. Formulations of Semisolid Drugs.2

Handbook of Pharmaceutical Manufacturing Formulations Second Edition

Bidang Ilmu : Farmasi

Penulis : Sarfaraz K. Niazi

Abstrak :

This Book is About Handbook of Pharmaceutical Manufacturing Formulations Second Edition.