The Comprehensive Guide To Clinical Research

The Comprehensive Guide To Clinical Research
Author :
Publisher : Independently Published
Total Pages : 218
Release :
ISBN-10 : 1090349521
ISBN-13 : 9781090349521
Rating : 4/5 (21 Downloads)

Synopsis The Comprehensive Guide To Clinical Research by : Chris Sauber

Condensing the most important topics in all of clinical research in an easy to understand presentation. The 20 percent of what you need to know in order to be 80 percent proficient!The authors who have operated various levels of businesses in the clinical research industry since 2005 believe that more practical information pertaining to clinical research needs to be accessible to individuals who are new to the industry or are curious about entering the rewarding world of clinical trials.This book reads in an easy to understand style and is based on proven methods the authors have developed to train their own employees and students of their various clinical research academies throughout the years. Picking this up and absorbing the information will allow anyone to gain much better insight into the complicated dynamics of clinical research. This practical roadmap is all you will need to get started on your clinical trial journey!In this book you will learn about:Regulations and the history as well as evolution of GCP.Clinical Research Site OperationsMonitoring Dynamics and Typical Monitoring VistsCRO ActivitiesSponsor Level DynamicsIndustry VendorsCommon Career Opportunities and Employment Roadmaps

The CRA's Guide to Monitoring Clinical Research

The CRA's Guide to Monitoring Clinical Research
Author :
Publisher : Centerwatch Incorporated
Total Pages : 454
Release :
ISBN-10 : 1930624557
ISBN-13 : 9781930624559
Rating : 4/5 (57 Downloads)

Synopsis The CRA's Guide to Monitoring Clinical Research by : Karen E. Woodin

A Clinical Trials Manual From The Duke Clinical Research Institute

A Clinical Trials Manual From The Duke Clinical Research Institute
Author :
Publisher : John Wiley & Sons
Total Pages : 381
Release :
ISBN-10 : 9781444357882
ISBN-13 : 1444357883
Rating : 4/5 (82 Downloads)

Synopsis A Clinical Trials Manual From The Duke Clinical Research Institute by : Margaret Liu

"The publication of the second edition of this manual comes at an important juncture in the history of clinical research. As advances in information technology make it possible to link individuals and groups in diverse locations in jointly seeking the answers to pressing global health problems, it is critically important to remain vigilant about moral and ethical safeguards for every patient enrolled in a trial. Those who study this manual will be well aware of how to ensure patient safety along with fiscal responsibility, trial efficiency, and research integrity." —Robert Harrington, Professor of Medicine, Director, Duke Clinical Research Institute, Durham, North Carolina, USA The Duke Clinical Research Institute (DCRI) is one of the world's leading academic clinical research organizations; its mission is to develop and share knowledge that improves the care of patients around the world through innovative clinical research. This concise handbook provides a practical "nuts and bolts" approach to the process of conducting clinical trials, identifying methods and techniques that can be replicated at other institutions and medical practices. Designed for investigators, research coordinators, CRO personnel, students, and others who have a desire to learn about clinical trials, this manual begins with an overview of the historical framework of clinical research, and leads the reader through a discussion of safety concerns and resulting regulations. Topics include Good Clinical Practice, informed consent, management of subject safety and data, as well as monitoring and reporting adverse events. Updated to reflect recent regulatory and clinical developments, the manual reviews the conduct of clinical trials research in an increasingly global context. This new edition has been further expanded to include: In-depth information on conducting clinical trials of medical devices and biologics The role and responsibilities of Institutional Review Boards, and Recent developments regarding subject privacy concerns and regulations. Ethical documents such as the Belmont Report and the Declaration of Helsinki are reviewed in relation to all aspects of clinical research, with a discussion of how researchers should apply the principles outlined in these important documents. This graphically appealing and eminently readable manual also provides sample forms and worksheets to facilitate data management and regulatory record retention; these can be modified and adapted for use at investigative sites.

Clinical Research Coordinator Handbook

Clinical Research Coordinator Handbook
Author :
Publisher : Plexus Publishing (UK)
Total Pages : 164
Release :
ISBN-10 : UOM:39015064104022
ISBN-13 :
Rating : 4/5 (22 Downloads)

Synopsis Clinical Research Coordinator Handbook by : Deborrah Norris

In this revised third edition of the essential reference for clinical research coordinators (CRCs), Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The book's five appendices include a directory of CRC resources, updated forms and checklists, state regulatory requirements and contact information, conversion charts and tables, a glossary, and more.

Emergency Response Guidebook

Emergency Response Guidebook
Author :
Publisher : Simon and Schuster
Total Pages : 352
Release :
ISBN-10 : 9781626363762
ISBN-13 : 1626363765
Rating : 4/5 (62 Downloads)

Synopsis Emergency Response Guidebook by : U.S. Department of Transportation

Does the identification number 60 indicate a toxic substance or a flammable solid, in the molten state at an elevated temperature? Does the identification number 1035 indicate ethane or butane? What is the difference between natural gas transmission pipelines and natural gas distribution pipelines? If you came upon an overturned truck on the highway that was leaking, would you be able to identify if it was hazardous and know what steps to take? Questions like these and more are answered in the Emergency Response Guidebook. Learn how to identify symbols for and vehicles carrying toxic, flammable, explosive, radioactive, or otherwise harmful substances and how to respond once an incident involving those substances has been identified. Always be prepared in situations that are unfamiliar and dangerous and know how to rectify them. Keeping this guide around at all times will ensure that, if you were to come upon a transportation situation involving hazardous substances or dangerous goods, you will be able to help keep others and yourself out of danger. With color-coded pages for quick and easy reference, this is the official manual used by first responders in the United States and Canada for transportation incidents involving dangerous goods or hazardous materials.

Theory at a Glance

Theory at a Glance
Author :
Publisher :
Total Pages : 52
Release :
ISBN-10 : MINN:31951D01539989F
ISBN-13 :
Rating : 4/5 (9F Downloads)

Synopsis Theory at a Glance by : Karen Glanz

Clinical Trials in Neurology

Clinical Trials in Neurology
Author :
Publisher : Cambridge University Press
Total Pages : 387
Release :
ISBN-10 : 9781107376571
ISBN-13 : 1107376572
Rating : 4/5 (71 Downloads)

Synopsis Clinical Trials in Neurology by : Bernard Ravina

Translating laboratory discoveries into successful therapeutics can be difficult. Clinical Trials in Neurology aims to improve the efficiency of clinical trials and the development of interventions in order to enhance the development of new treatments for neurologic diseases. It introduces the reader to the key concepts underpinning trials in the neurosciences. This volume tackles the challenges of developing therapies for neurologic disorders from measurement of agents in the nervous system to the progression of clinical signs and symptoms through illustrating specific study designs and their applications to different therapeutic areas. Clinical Trials in Neurology covers key issues in Phase I, II and III clinical trials, as well as post-marketing safety surveillance. Topics addressed include regulatory and implementation issues, outcome measures and common problems in drug development. Written by a multidisciplinary team, this comprehensive guide is essential reading for neurologists, psychiatrists, neurosurgeons, neuroscientists, statisticians and clinical researchers in the pharmaceutical industry.

Oncology Clinical Trials

Oncology Clinical Trials
Author :
Publisher : Demos Medical Publishing
Total Pages : 396
Release :
ISBN-10 : 9781935281764
ISBN-13 : 1935281763
Rating : 4/5 (64 Downloads)

Synopsis Oncology Clinical Trials by : Susan Halabi, PhD

Clinical trials are the engine of progress in the development of new drugs and devices for the detection, monitoring, prevention and treatment of cancer. A well conceived, carefully designed and efficiently conducted clinical trial can produce results that change clinical practice overnight, deliver new oncology drugs and diagnostics to the marketplace, and expand the horizon of contemporary thinking about cancer biology. A poorly done trial does little to advance the field or guide clinical practice, consumes precious clinical and financial resources and challenges the validity of the ethical contract between investigators and the volunteers who willingly give their time and effort to benefit future patients. With chapters written by oncologists, researchers, biostatisticians, clinical research administrators, and industry and FDA representatives, Oncology Clinical Trials, provides a comprehensive guide for both early-career and senior oncology investigators into the successful design, conduct and analysis of an oncology clinical trial. Oncology Clinical Trials covers how to formulate a study question, selecting a study population, study design of Phase I, II, and III trials, toxicity monitoring, data analysis and reporting, use of genomics, cost-effectiveness analysis, systemic review and meta-analysis, and many other issues. Many examples of real-life flaws in clinical trials that have been reported in the literature are included throughout. The book discusses clinical trials from start to finish focusing on real-life examples in the development, design and analysis of clinical trials. Oncology Clinical Trials features: A systematic guide to all aspects of the design, conduct, analysis, and reporting of clinical trials in oncology Contributions from oncologists, researchers, biostatisticians, clinical research administrators, and industry and FDA representatives Hot topics in oncology trials including multi-arm trials, meta-analysis and adaptive design, use of genomics, and cost-effectiveness analysis Real-life examples from reported clinical trials included throughout