Patient Recruitment In Clinical Research
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Reinventing Patient Recruitment
Author | : Joan F. Bachenheimer,Bonnie A. Brescia |
Publsiher | : Routledge |
Total Pages | : 278 |
Release | : 2017-03-02 |
Genre | : Business & Economics |
ISBN | : 9781351905237 |
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During the last five years, clinical research and development costs have risen exponentially without a proportionate increase in the number of new medications. While patient recruitment for clinical studies is only one component in the development of a new medicine or treatment, it is one of the most significant bottlenecks in the overall drug development process. Now it is imperative that industry leaders see beyond reactive measures and recognize that advancing their approach to patient recruitment is absolutely essential to advancing medicine and continuing the stability of their corporate brand across the globe. Reinventing Patient Recruitment: Revolutionary Ideas for Clinical Trial Success is a definitive guide to planning, implementing and evaluating recruitment strategies and campaigns globally. The combined experience of the authors provides a depth of perspective and boldness of innovative leadership to set the standards for future patient recruitment programs and practices. This book is a must-have for pharmaceutical, biotechnology and medical device industry professionals concerned with enrolling for domestic and multinational clinical studies and remaining on time and on budget.
A Guide to Patient Recruitment and Retention
Author | : Diana L. Anderson (Ph.D.) |
Publsiher | : CenterWatch |
Total Pages | : 314 |
Release | : 2004 |
Genre | : Clinical trials |
ISBN | : UCLA:L0089427603 |
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Patient recruitment and retention are clearly complex and challenging components of the clinical trials process. In the industry's foremost resource, A Guide to Patient Recruitment and Retention, the authors provide a wealth of practical advice and quantifiable examples on every aspect of patient recruitment. This book builds on the success of the original -- A Guide to Patient Recruitment -- by introducing many innovative, multi-faceted strategies designed to recruit and retain patients in clinical trials. Book jacket.
Patient Recruitment in Clinical Research
Author | : Danielle Jacobs |
Publsiher | : Inst of Clinical Research |
Total Pages | : 48 |
Release | : 2005 |
Genre | : Clinical trials |
ISBN | : 9780954934538 |
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Provides ideas for how to improve patient recruitment for clinical trials.
Accelerating Patient Recruitment in Clinical Trials
Author | : Anonim |
Publsiher | : NetworkPharma Ltd |
Total Pages | : 20 |
Release | : 2006 |
Genre | : Clinical trials |
ISBN | : 9781905676071 |
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Neuroscience Trials of the Future
Author | : National Academies of Sciences, Engineering, and Medicine,Health and Medicine Division,Board on Health Sciences Policy,Forum on Neuroscience and Nervous System Disorders |
Publsiher | : National Academies Press |
Total Pages | : 111 |
Release | : 2016-11-07 |
Genre | : Medical |
ISBN | : 9780309442589 |
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On March 3-4, 2016, the National Academies of Sciences, Engineering, and Medicine's Forum on Neuroscience and Nervous System Disorders held a workshop in Washington, DC, bringing together key stakeholders to discuss opportunities for improving the integrity, efficiency, and validity of clinical trials for nervous system disorders. Participants in the workshop represented a range of diverse perspectives, including individuals not normally associated with traditional clinical trials. The purpose of this workshop was to generate discussion about not only what is feasible now, but what may be possible with the implementation of cutting-edge technologies in the future.
Patient Recruitment in Clinical Trials
Author | : Bert Spilker,Joyce A. Cramer |
Publsiher | : Raven Press (ID) |
Total Pages | : 376 |
Release | : 1992 |
Genre | : Health & Fitness |
ISBN | : UOM:39015028426859 |
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A step-by-step guide to developing and implementing a strategy for successful patient recruitment. It details practical approaches to preventing or solving the problems that can arise in every phase of the recruitment process. Samples of advertisements, brochures and other materials are included.
Virtual Clinical Trials
Author | : National Academies of Sciences, Engineering, and Medicine,Health and Medicine Division,Board on Health Sciences Policy,Forum on Drug Discovery, Development, and Translation |
Publsiher | : National Academies Press |
Total Pages | : 127 |
Release | : 2019-11-16 |
Genre | : Medical |
ISBN | : 9780309494885 |
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Successful drug development relies on accurate and efficient clinical trials to deliver the best and most effective pharmaceuticals and clinical care to patients. However, the current model for clinical trials is outdated, inefficient and costly. Clinical trials are limited by small sample sizes that do not reflect variations among patients in the real world, financial burdens on participants, and slow processes, and these factors contribute to the disconnect between clinical research and clinical practice. On November 28-29, the National Academies of Sciences, Engineering, and Medicine convened a workshop to investigate the current clinical trials system and explore the potential benefits and challenges of implementing virtual clinical trials as an enhanced alternative for the future. This publication summarizes the presentations and discussions from the workshop.
Sharing Clinical Trial Data
Author | : Institute of Medicine,Board on Health Sciences Policy,Committee on Strategies for Responsible Sharing of Clinical Trial Data |
Publsiher | : National Academies Press |
Total Pages | : 304 |
Release | : 2015-04-20 |
Genre | : Medical |
ISBN | : 9780309316323 |
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Data sharing can accelerate new discoveries by avoiding duplicative trials, stimulating new ideas for research, and enabling the maximal scientific knowledge and benefits to be gained from the efforts of clinical trial participants and investigators. At the same time, sharing clinical trial data presents risks, burdens, and challenges. These include the need to protect the privacy and honor the consent of clinical trial participants; safeguard the legitimate economic interests of sponsors; and guard against invalid secondary analyses, which could undermine trust in clinical trials or otherwise harm public health. Sharing Clinical Trial Data presents activities and strategies for the responsible sharing of clinical trial data. With the goal of increasing scientific knowledge to lead to better therapies for patients, this book identifies guiding principles and makes recommendations to maximize the benefits and minimize risks. This report offers guidance on the types of clinical trial data available at different points in the process, the points in the process at which each type of data should be shared, methods for sharing data, what groups should have access to data, and future knowledge and infrastructure needs. Responsible sharing of clinical trial data will allow other investigators to replicate published findings and carry out additional analyses, strengthen the evidence base for regulatory and clinical decisions, and increase the scientific knowledge gained from investments by the funders of clinical trials. The recommendations of Sharing Clinical Trial Data will be useful both now and well into the future as improved sharing of data leads to a stronger evidence base for treatment. This book will be of interest to stakeholders across the spectrum of research--from funders, to researchers, to journals, to physicians, and ultimately, to patients.