Drugs
(Sprache: Englisch)
The new edition of this best-selling book continues to offer a user-friendly, step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of pre-clinical studies, the conduct of human clinical...
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The new edition of this best-selling book continues to offer a user-friendly, step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of pre-clinical studies, the conduct of human clinical trials, regulatory controls, and even the manufacturing processes for pharmaceutical products. Concise and easy to read, the book quickly introduces basic concepts, then moves on to discuss target selection and the drug discovery process for both small and large molecular drugs. The new edition features many key enhancements, including Key Points, Chapter Summary, and Review Questions in each chapter, Answers to Review Questions provided in a book-end appendix, and one or two carefully selected "mini" case studies in each chapter.
The new edition of this best-selling book continues to offer a user-friendly, step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of pre-clinical studies, the conduct of human clinical trials, regulatory controls, and even the manufacturing processes for pharmaceutical products. Concise and easy to read, the book quickly introduces basic concepts, then moves on to discuss target selection and the drug discovery process for both small and large molecular drugs. The new edition features many key enhancements, including Key Points, Chapter Summary, and Review Questions in each chapter, Answers to Review Questions provided in a book-end appendix, and one or two carefully selected "mini" case studies in each chapter.
Inhaltsverzeichnis zu „Drugs “
PREFACE1 INTRODUCTION
2 DRUG DISCOVERY: TARGETS AND RECEPTORS
3 DRUG DISCOVERY: SMALL MOLECULE DRUGS
4 DRUG DISCOVERY: LARGE MOLECULE DRUGS
5 DRUG DEVELOPMENT AND PRECLINICAL STUDIES
6 CLINICAL TRIALS
7 REGULATORY AUTHORITIES
8 REGULATORY APPLICATIONS
9 GOOD MANUFACTURING PRACTICE: REGULATORY REQUIREMENT
10 GOOD MANUFACTURING PRACTICE: DRUG MANUFACTURING
11 FUTURE PERSPECTIVES
APPENDIX 1 HISTORY OF DRUG DISCOVERY AND DEVELOPMENT
APPENDIX 2 CELLS, NUCLEIC ACIDS, GENES, AND PROTEINS
APPENDIX 3 SELECTED DRUGS AND THEIR MECHANISMS OF ACTION
APPENDIX 4 A DHFR PLASMID VECTOR
APPENDIX 5 VACCINE PRODUCTION METHODS
APPENDIX 6 PHARMACOLOGY/ TOXICOLOGY
REVIEW FORMAT
APPENDIX 7 EXAMPLES OF GENERAL BIOMARKERS
APPENDIX 8 TOXICITY GRADING
APPENDIX 9 HEALTH SYSTEMS IN SELECTED COUNTRIES
ACRONYMS
GLOSSARY
INDEX
Autoren-Porträt von Rick Ng
Rick Ng, PhD, has worked for more than twenty-five years in senior management positions in the private sector pharmaceutical industry. He is currently a director at a biopharmaceutical manufacturing facility in Singapore. He has provided technical training for graduate and postgraduate personnel.
Bibliographische Angaben
- Autor: Rick Ng
- 2008, 2. Aufl., 472 Seiten, Maße: 23,8 cm, Gebunden, Englisch
- Verlag: Wiley & Sons
- ISBN-10: 047019510X
- ISBN-13: 9780470195109
Sprache:
Englisch
Rezension zu „Drugs “
"The second edition of a book that offers a user-friendly step-by-step introduction to all the key processes involved in bringing a drug to the market, including the performance of preclinical trials." (Chemistry World, February 2009)
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