Nonclinical Assessment of Abuse Potential for New Pharmaceuticals

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  • Author : Carrie Markgraf
  • Publisher : Academic Press
  • Pages : 320 pages
  • ISBN : 9780124201729
  • Rating : /5 from reviews
CLICK HERE TO GET THIS BOOK >>>Nonclinical Assessment of Abuse Potential for New Pharmaceuticals

Download or Read online Nonclinical Assessment of Abuse Potential for New Pharmaceuticals full in PDF, ePub and kindle. this book written by Carrie Markgraf and published by Academic Press which was released on 01 August 2015 with total page 320 pages. We cannot guarantee that Nonclinical Assessment of Abuse Potential for New Pharmaceuticals book is available in the library, click Get Book button and read full online book in your kindle, tablet, IPAD, PC or mobile whenever and wherever You Like. Nonclinical Assessment of Abuse Potential for New Pharmaceuticals offers a complete reference on the current international regulatory guidelines and details best practice methodology for the three standard animal models used to evaluate abuse potential: physical dependence, self-administration and drug discrimination. This book also includes chapters on alternative models and examples of when you should use these alternatives. Case histories are provided at the end of the book to show how the data generated from the animal models play a pivitol role in the submission package for a new drug. By incorporating all of this information into one book, Nonclinical Assessment of Abuse Potential for New Pharmaceuticals is your single resource for everything you need to know to understand and implement the assessment of abuse liability. Provides a consolidated overview of the complex regulatory landscape Offers best practice methodology for conducting animal studies, including selection of doses and positive control agents that will help you improve your own abuse potential studies Includes real-life examples to illustrate how nonclinical data fit into the submission strategy

Nonclinical Assessment of Abuse Potential for New Pharmaceuticals

Nonclinical Assessment of Abuse Potential for New Pharmaceuticals
  • Author : Carrie Markgraf,Thomas Hudzik,David Compton
  • Publisher : Academic Press
  • Release : 01 August 2015
GET THIS BOOK Nonclinical Assessment of Abuse Potential for New Pharmaceuticals

Nonclinical Assessment of Abuse Potential for New Pharmaceuticals offers a complete reference on the current international regulatory guidelines and details best practice methodology for the three standard animal models used to evaluate abuse potential: physical dependence, self-administration and drug discrimination. This book also includes chapters on alternative models and examples of when you should use these alternatives. Case histories are provided at the end of the book to show how the data generated from the animal models play a pivitol

Nonclinical Assessment of Abuse Potential for New Pharmaceuticals

Nonclinical Assessment of Abuse Potential for New Pharmaceuticals
  • Author : Carrie Markgraf,Thomas Hudzik,David Compton
  • Publisher : Academic Press
  • Release : 14 July 2015
GET THIS BOOK Nonclinical Assessment of Abuse Potential for New Pharmaceuticals

Nonclinical Assessment of Abuse Potential for New Pharmaceuticals offers a complete reference on the current international regulatory guidelines and details best practice methodology for the three standard animal models used to evaluate abuse potential: physical dependence, self-administration and drug discrimination. This book also includes chapters on alternative models and examples of when you should use these alternatives. Case histories are provided at the end of the book to show how the data generated from the animal models play a pivitol

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A Comprehensive Guide to Toxicology in Nonclinical Drug Development
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  • Publisher : Academic Press
  • Release : 03 November 2016
GET THIS BOOK A Comprehensive Guide to Toxicology in Nonclinical Drug Development

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  • Publisher : Academic Press
  • Release : 18 October 2012
GET THIS BOOK A Comprehensive Guide to Toxicology in Preclinical Drug Development

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  • Release : 13 October 2016
GET THIS BOOK Stem Cells in Toxicology and Medicine

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  • Publisher : Academic Press
  • Release : 13 March 2015
GET THIS BOOK The Nonhuman Primate in Nonclinical Drug Development and Safety Assessment

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  • Publisher : Oxford University Press, USA
  • Release : 01 October 2020
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"Over the last few years there has been an increased interest in identification and treatment of substance use disorders, due at least in part to the widespread drug overdose epidemic. Clinicians and the lay public have gained a greater understanding of the need for treatment of substance use disorders and the consequences of avoiding treatment. In addition, there has been a growing understanding of substance use disorders as medical or mental health disorders, rather than character flaws or merely illegal

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  • Publisher : CRC Press
  • Release : 21 November 2019
GET THIS BOOK Drug Discovery and Development Third Edition

Drug Discovery and Development, Third Edition presents up-to-date scientific information for maximizing the ability of a multidisciplinary research team to discover and bring new drugs to the marketplace. It explores many scientific advances in new drug discovery and development for areas such as screening technologies, biotechnology approaches, and evaluation of efficacy and safety of drug candidates through preclinical testing. This book also greatly expands the focus on the clinical pharmacology, regulatory, and business aspects of bringing new drugs to the

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  • Publisher : Academic Press
  • Release : 16 May 2020
GET THIS BOOK Information Resources in Toxicology

This new fifth edition of Information Resources in Toxicology offers a consolidated entry portal for the study, research, and practice of toxicology. Both volumes represents a unique, wide-ranging, curated, international, annotated bibliography, and directory of major resources in toxicology and allied fields such as environmental and occupational health, chemical safety, and risk assessment. The editors and authors are among the leaders of the profession sharing their cumulative wisdom in toxicology’s subdisciplines. This edition keeps pace with the digital world

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GET THIS BOOK The SAGE Encyclopedia of Pharmacology and Society

The SAGE Encyclopedia of Pharmacology and Society explores the social and policy sides of the pharmaceutical industry and its pervasive influence in society. While many technical STM works explore the chemistry and biology of pharmacology and an equally large number of clinically oriented works focus on use of illegal drugs, substance abuse, and treatment, there is virtually nothing on the immensely huge business (“Big Pharma”) of creating, selling, consuming, and regulating legal drugs. With this new Encyclopedia, the topic of

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  • Publisher : Springer
  • Release : 19 June 2015
GET THIS BOOK Principles of Safety Pharmacology

This book illustrates, in a comprehensive manner, the most current areas of importance to Safety Pharmacology, a burgeoning unique pharmacological discipline with important ties to academia, industry and regulatory authorities. It provides readers with a definitive collection of topics containing essential information on the latest industry guidelines and overviews current and breakthrough topics in both functional and molecular pharmacology. An additional novelty of the book is that it constitutes academic, pharmaceutical and biotechnology perspectives for Safety Pharmacology issues. Each chapter

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  • Publisher : Academic Press
  • Release : 05 September 2018
GET THIS BOOK Advanced Issue Resolution in Safety Pharmacology

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  • Release : 15 March 2012
GET THIS BOOK Veterinary Toxicology

Veterinary Toxicology is a unique single reference that teaches the basic principles of veterinary toxicology to any student at the DVM, MS or PhD level and will continue to serve as a clinical reference for practicing veterinary toxicologists, poison control centers, marine biologists, environmentalists, and animal scientists. While most comparable texts are primarily directed toward the field of human toxicology, this is the one text needed to thoroughly prepare future veterinarians on the newest approaches for diagnosing poisoning cases in

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  • Release : 02 May 2014
GET THIS BOOK The Role of the Study Director in Nonclinical Studies

A single-source reference with a broad and holistic overview of nonclinical studies, this book offers critical training material and describes regulations of nonclinical testing through guidelines, models, case studies, practical examples, and worldwide perspectives. The book: Provides a complete overview of nonclinical study organization, conduct, and reporting and describes the roles and responsibilities of a Study Director to manage an effective study Covers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, and animal

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GET THIS BOOK Drug Discovery and Development

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