New Drug Development
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New Drug Development
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Author : J. Rick Turner
language : en
Publisher: Springer Science & Business Media
Release Date : 2010-07-16
New Drug Development written by J. Rick Turner and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2010-07-16 with Medical categories.
New Drug Development: Second Edition provides an overview of the design concepts and statistical practices involved in therapeutic drug development. This wide spectrum of activities begins with identifying a potentially useful drug candidate that can perhaps be used in the treatment or prevention of a condition of clinical concern, and ends with marketing approval being granted by one or more regulatory agencies. In between, it includes drug molecule optimization, nonclinical and clinical evaluations of the drug’s safety and efficacy profiles, and manufacturing considerations. The more inclusive term lifecycle drug development can be used to encompass the postmarketing surveillance that is conducted all the time that a drug is on the market and being prescribed to patients with the relevant clinical condition. Information gathered during this time can be used to modify the drug (for example, dose prescribed, formulation, and mode of administration) in terms of its safety and its effectiveness. The central focus of the first edition of this book is captured by its subtitle, 'Design, Methodology, and Analysis'. Optimum quality study design and experimental research methodology must be employed if the data collected—numerical representations of biological information—are to be of optimum quality. Optimum quality data facilitate optimum quality statistical analysis and interpretation of the results obtained, which in turn permit optimum quality decisions to be made: Rational decision making is predicated on appropriate research questions and optimum quality numerical information. The book took a non-computational approach to statistics, presenting instead a conceptual framework and providing readers with a sound working knowledge of the importance of design, methodology, and analysis. Not everyone needs to be an expert in statistical analysis, but it is very helpful for work (or aspire to work) in the pharmaceutical and biologics industries to be aware of the fundamental importance of a sound scientific and clinical approach to the planning, conduct, and analysis of clinical trials.
From Test Tube To Patient
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Author :
language : en
Publisher:
Release Date : 1995
From Test Tube To Patient written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1995 with Clinical pharmacology categories.
Global New Drug Development
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Author : Jan A. Rosier
language : en
Publisher: John Wiley & Sons
Release Date : 2014-07-03
Global New Drug Development written by Jan A. Rosier and has been published by John Wiley & Sons this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014-07-03 with Medical categories.
The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of the drug life cycle, drug development is by far the most crucial part for the initial and continued success of a drug on the market. This book offers an introduction to the field of drug development with a clear overview of the different processes that lead to a successful new medicine and of the regulatory pathways that are used to launch a new drug that are both safe and efficacious. "This is the most comprehensive and detailed book on drug development I have ever read and I feel that it is likely to become a staple of drug development courses, such as those taught at Masters Level in my own University.... I think in the light of increasing integration of company and academic approaches to drug development both sides can read this book... (and, therefore)... this book could not be more timely." —Professor Mike Coleman, University of Aston, UK ( from his review of the final manuscript)
From Test Tube To Patient
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Author : DIANE Publishing Company
language : en
Publisher: DIANE Publishing
Release Date : 1995-07
From Test Tube To Patient written by DIANE Publishing Company and has been published by DIANE Publishing this book supported file pdf, txt, epub, kindle and other format this book has been release on 1995-07 with categories.
Covers: laboratory and animal studies, testing in "real people", experimental drugs, watching for problems, myths and facts of generic drugs, and much more. Illustrated.
New Drug Development
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Author : Mark P. Mathieu
language : en
Publisher: Parexel International Corporation
Release Date : 1990
New Drug Development written by Mark P. Mathieu and has been published by Parexel International Corporation this book supported file pdf, txt, epub, kindle and other format this book has been release on 1990 with Drugs categories.
New Drug Development Science Business Regulatory Intellectual Property Issues Cited As Hampering Drug Development Efforts
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Author : United States Government Accountability Office
language : en
Publisher: DIANE Publishing
Release Date : 2006
New Drug Development Science Business Regulatory Intellectual Property Issues Cited As Hampering Drug Development Efforts written by United States Government Accountability Office and has been published by DIANE Publishing this book supported file pdf, txt, epub, kindle and other format this book has been release on 2006 with categories.
Simultaneous Global New Drug Development
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Author : Gang Li
language : en
Publisher: CRC Press
Release Date : 2021-12-15
Simultaneous Global New Drug Development written by Gang Li and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-12-15 with Mathematics categories.
Global simultaneous development is becoming more necessary as the cost of developing medical products continues to grow. The strategy of using multiregional clinical trials (MRCTs) has become the preferred method for developing new medicines. Implementing the same protocol to include subjects from many geographical regions around the world, MRCTs can speed up the patient enrolment, thus resulting in quicker drug development and obtaining faster approval of the drug globally. After the publication of the editors’ first volume on this topic, there have been new developments on MRCTs. The International Council for Harmonisation (ICH) issued ICH E17, a guideline document on MRCTs, in November 2017, laying out principles on MRCTs. Beyond E17, new methodologies have been developed as well. Simultaneous Global New Drug Development: Multi-Regional Clinical Trials after ICH E17 collects chapters providing interpretations of principles in ICH E17 and new ideas of implementing MRCTs. Authors are from different regions, and from academia and industry. In addition, in contrast to the first book, new perspectives are brought to MRCT from regulatory agencies. This book will be of particular interest to biostatisticians working in late stage clinical development of medical products. It will also be especially helpful for statisticians in regulatory agencies, and medical research institutes. This book is comprehensive across the MRCT topic spectrum, including Issues regarding ICH E17 Implementation MRCT Design and Analysis Methodologies Perspectives from authorities in regulatory agencies, as well as statisticians practicing in the medical product industry Many examples of real-life applications based on actual MRCTs.
New Drug Approval Process
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Author : Richard A. Guarino
language : en
Publisher: CRC Press
Release Date : 2016-04-19
New Drug Approval Process written by Richard A. Guarino and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-04-19 with Medical categories.
The thoroughly revised Fifth Edition of New Drug Approval Process supplies readers with the latest global changes that affect pharmaceutical product approval and influence how new products are researched and marketed.Updated chapters include:advances in international regulatory requirements, including ICH guidelines and harmonizationa step-by-step
New Drug Development
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Author : Mark P. Mathieu
language : en
Publisher: Parexel International Corporation
Release Date : 1997
New Drug Development written by Mark P. Mathieu and has been published by Parexel International Corporation this book supported file pdf, txt, epub, kindle and other format this book has been release on 1997 with Business & Economics categories.
New Drug Development
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Author : Mark P. Mathieu
language : en
Publisher: Omec
Release Date : 1987
New Drug Development written by Mark P. Mathieu and has been published by Omec this book supported file pdf, txt, epub, kindle and other format this book has been release on 1987 with Medical categories.