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Pharmaceutical Bioequivalence
The rate and extent of drug absorption are a function of many factors, including the site of adminis;...
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Pharmaceutical Statistics
Through the use of practical examples and solutions, Pharmaceutical Statistics: Practical and Clinical Applications, Fifth Edition;
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Statistics in Drug Research
applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation and;
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Statistics in Drug Research
applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation and;
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Generic Drug Product Development
-name counterpart. Generic pharmaceutical products must be approved as therapeutic equivalents to the brand name alternative in order to be;
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Bioequivalence and Statistics in Clinical Pharmacology
demonstrates the methods using real world examples. Drawing on knowledge gained directly from working in the pharmaceutical industry, the authors;
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Bioequivalence and Statistics in Clinical Pharmacology
demonstrates the methods using real world examples. Drawing on knowledge gained directly from working in the pharmaceutical industry, the;
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Modern Pharmaceutics, Volume 2
. In addition, this text discusses the impact of the shift to personalized medicines in the fields of pharmaceutical biotechnology, pharmacogenomics;
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Generic Drug Product Development
Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;
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Generic Drug Product Development
Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;
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Pharmaceutical Statistics
spectrum of pharmaceutical R&D - with a special focus on emergent topics such as biosimilarity, bioequivalence, clinical trial design, and subgroup;
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Pharmaceutical Quality by Design
Pharmaceutical Quality by Design: Principles and Applications discusses the Quality by Design (QbD) concept implemented by regulatory;
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Bioequivalence and Statistics in Clinical Pharmacology
directly from working in the pharmaceutical industry, the authors set the stage by describing the general role of statistics. Once the foundation;
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Pharmaceutical Dissolution Testing
Introduction, Historical Highlights, and the Need for Dissolution Testing Theories of Dissolution Di;...
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Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition
In this era of increased pharmaceutical industry competition, success for generic drug companies is dependent on their ability to;
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Bio Equivalence Study on Omeprazole 20mg Powder for Suspension
Bioequivalence studies conduct for the comparison of two medicinal products containing the same acti;...
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Design and Analysis of Bioavailability and Bioequivalence Studies
Preeminent Experts Update a Well-Respected Book Taking into account the regulatory and scientific de;...
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Design and Analysis of Bioavailability and Bioequivalence Studies
Preeminent Experts Update a Well-Respected Book Taking into account the regulatory and scientific;...
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Clinical Trial Methodology
on the subject as well as the first author's more than 30 years working in the pharmaceutical industry, Clinical Trial Methodology emphasizes;
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Clinical Trial Methodology
on the subject as well as the first author's more than 30 years working in the pharmaceutical industry, Clinical Trial Methodology emphasizes;
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two, Uncompressed Solid Products is an authoritative and;
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile Products is an authoritative and practical;
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Five, Over-the-Counter Products is an authoritative and;
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Handbook of Pharmaceutical Manufacturing Formulations, Third Edition
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products is an authoritative and practical;
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Developing Solid Oral Dosage Forms
Developing Solid Oral Dosage Forms: Pharmaceutical Theory and Practice, Second Edition illustrates how to develop high-quality, safe;
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Topical Drug Bioavailability, Bioequivalence, and Penetration
This authoritative volume explores advances in the techniques used to measure percutaneous penetrati;...
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