Social Aspects of Drug Discovery, Development and Commercialization provides an insightful analysis of the drug discovery and development landscape as it relates to society. This book examines the scientific, legal, philosophical, economic, political, ethical and cultural factors that contribute to drug development. The pharmaceutical industry is under scrutiny to develop safer and more effective drugs in a quicker and more affordable manner. Recent criticism and debates have emphasized varying opinions on the issues concerning the drug discovery and development process.
This book provides thoughtful and valuable discussions and analysis of the social challenges and potential opportunities through all stages of the pharmaceutical process, from inception through marketing. With a unique focus on the social factors that increasingly play a role in how drug development is planned, structured, and executed throughout the drug product lifecycle, this is an essential resource for students, professors, and researchers who seek a better understanding of the interface between the pharmaceutical industry, health care systems, and society.
- Organized in a sequence of interrelated theories and principles that provide the foundation for increased understanding of the relevant social aspects
- Includes analysis of important new advances, key scientific and strategic issues, and overviews of recent progress in drug development
- Provides a global perspective with examples from developed areas, such as the US, Japan, Canada and Europe, as well as faster-growing and emerging economies including Brazil, Russia, India, and China
- Serves as an essential resource for students, professors, and researchers who seek a better understanding of the interface between the pharmaceutical industry, health care systems, and society
Dr. Odilia Osakwe has published 25 titles, including 1 book (edited), 24 articles in peer reviewed platform including journal articles, scholarly magazines, newsletters and technical notes. And has authored 10 papers/posters and oral presentations in major international professional meetings. Odilia has reviewed numerous manuscripts for different academic journals. Aside from those activities, she served as an editorial board member with Pharmaceutical Science Group of Canada for 3 years reviewing and editing articles with active contribution towards several of the published front cover topics. Odilia received her undergraduate degree from Abia state University and her Masters in Chemistry from Tennessee State University. Within this period, she worked with the Tennessee State Department of Laboratory Services. Following completion of a Master Degree in Chemistry, she took on a two-year post graduate fellowship, which was granted by Vanderbilt University, Nashville, Tennessee; completed in the department of pharmacology of Vanderbilt University Medical Centre. She joined a doctoral program with the department of pharmaceutical Sciences of Mercer University, Atlanta, Georgia and earned a PhD degree. During much of this period, starting from the second year into the doctoral program, she joined the Georgia Perimeter College, Atlanta, Georgia, teaching Chemistry courses for two years till the end of the program. During the all-but-dissertation stage, (ABD), Odilia received a Student Research Fellowship with the Centers for Disease Control and Prevention (CDC), Atlanta, Georgia where she worked as a researcher with the immunology laboratories of National Center for Immunization and Respiratory Diseases (NCIRD) in the Division of Bacterial Diseases (DBD), using the state-of-the-art instrumentation for validation of immunological assays. Further on, Odilia received a competitive National Science and Engineering Research Council of Canada (NSERC) award for Industrial Research and Development Postdoctoral Fellowship (IRDF-NSERC). The two-year training was accomplished at the University of Toronto Hospital Network, Industrial BioDevelopment Laboratory (IBDL) department where she took the lead of the Research and Development activities which include technical oversight and training of the University of Toronto undergraduates on various projects, with published results. Odilia works with Devik Pharma Inc., also a board member of the North American Institute of Pharmaceutical Technology, Scarborough, Ontario, Canada where she undertakes administrative and scholarly duties in the industrial pharmaceutical sector. She is an Adjunct Faculty with Ryerson University, Toronto, Ontario, Canada and Seneca College of Arts and Technology, Toronto, Ontario, Canada, teaching several courses in the Industrial Pharmaceutical Technology program.
Social Aspects of Drug Discovery, Development and Commercialization provides an insightful analysis of the drug discovery and development landscape as it relates to society. This book examines the scientific, legal, philosophical, economic, political, ethical and cultural factors that contribute to drug development. The pharmaceutical industry is under scrutiny to develop safer and more effective drugs in a quicker and more affordable manner. Recent criticism and debates have emphasized varying opinions on the issues concerning the drug discovery and development process. This book provides thoughtful and valuable discussions and analysis of the social challenges and potential opportunities through all stages of the pharmaceutical process, from inception through marketing. With a unique focus on the social factors that increasingly play a role in how drug development is planned, structured, and executed throughout the drug product lifecycle, this is an essential resource for students, professors, and researchers who seek a better understanding of the interface between the pharmaceutical industry, health care systems, and society. Organized in a sequence of interrelated theories and principles that provide the foundation for increased understanding of the relevant social aspects Includes analysis of important new advances, key scientific and strategic issues, and overviews of recent progress in drug development Provides a global perspective with examples from developed areas, such as the US, Japan, Canada and Europe, as well as faster-growing and emerging economies including Brazil, Russia, India, and China Serves as an essential resource for students, professors, and researchers who seek a better understanding of the interface between the pharmaceutical industry, health care systems, and society
Erscheint lt. Verlag | 1.3.2016 |
---|---|
Sprache | englisch |
Themenwelt | Medizin / Pharmazie ► Gesundheitsfachberufe |
Medizin / Pharmazie ► Medizinische Fachgebiete ► Pharmakologie / Pharmakotherapie | |
Naturwissenschaften | |
ISBN-10 | 0-12-802497-6 / 0128024976 |
ISBN-13 | 978-0-12-802497-3 / 9780128024973 |
Haben Sie eine Frage zum Produkt? |
Größe: 9,1 MB
Kopierschutz: Adobe-DRM
Adobe-DRM ist ein Kopierschutz, der das eBook vor Mißbrauch schützen soll. Dabei wird das eBook bereits beim Download auf Ihre persönliche Adobe-ID autorisiert. Lesen können Sie das eBook dann nur auf den Geräten, welche ebenfalls auf Ihre Adobe-ID registriert sind.
Details zum Adobe-DRM
Dateiformat: PDF (Portable Document Format)
Mit einem festen Seitenlayout eignet sich die PDF besonders für Fachbücher mit Spalten, Tabellen und Abbildungen. Eine PDF kann auf fast allen Geräten angezeigt werden, ist aber für kleine Displays (Smartphone, eReader) nur eingeschränkt geeignet.
Systemvoraussetzungen:
PC/Mac: Mit einem PC oder Mac können Sie dieses eBook lesen. Sie benötigen eine
eReader: Dieses eBook kann mit (fast) allen eBook-Readern gelesen werden. Mit dem amazon-Kindle ist es aber nicht kompatibel.
Smartphone/Tablet: Egal ob Apple oder Android, dieses eBook können Sie lesen. Sie benötigen eine
Geräteliste und zusätzliche Hinweise
Buying eBooks from abroad
For tax law reasons we can sell eBooks just within Germany and Switzerland. Regrettably we cannot fulfill eBook-orders from other countries.
Größe: 5,4 MB
Kopierschutz: Adobe-DRM
Adobe-DRM ist ein Kopierschutz, der das eBook vor Mißbrauch schützen soll. Dabei wird das eBook bereits beim Download auf Ihre persönliche Adobe-ID autorisiert. Lesen können Sie das eBook dann nur auf den Geräten, welche ebenfalls auf Ihre Adobe-ID registriert sind.
Details zum Adobe-DRM
Dateiformat: EPUB (Electronic Publication)
EPUB ist ein offener Standard für eBooks und eignet sich besonders zur Darstellung von Belletristik und Sachbüchern. Der Fließtext wird dynamisch an die Display- und Schriftgröße angepasst. Auch für mobile Lesegeräte ist EPUB daher gut geeignet.
Systemvoraussetzungen:
PC/Mac: Mit einem PC oder Mac können Sie dieses eBook lesen. Sie benötigen eine
eReader: Dieses eBook kann mit (fast) allen eBook-Readern gelesen werden. Mit dem amazon-Kindle ist es aber nicht kompatibel.
Smartphone/Tablet: Egal ob Apple oder Android, dieses eBook können Sie lesen. Sie benötigen eine
Geräteliste und zusätzliche Hinweise
Buying eBooks from abroad
For tax law reasons we can sell eBooks just within Germany and Switzerland. Regrettably we cannot fulfill eBook-orders from other countries.
aus dem Bereich