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A Guide to Patient Recruitment and Retention

2004 Clinical trials
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Release : 2004
Genre : Clinical trials
Kind : eBook
Book Rating : /5 ( reviews)

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Book Synopsis A Guide to Patient Recruitment and Retention by : Diana L. Anderson (Ph.D.)

Download or read book A Guide to Patient Recruitment and Retention written by Diana L. Anderson (Ph.D.). This book was released on 2004. Available in PDF, EPUB and Kindle. Book excerpt: 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.

A Guide to Patient Recruitment

2001 Clinical trials
Download A Guide to Patient Recruitment PDF Online Free

Author :
Release : 2001
Genre : Clinical trials
Kind : eBook
Book Rating : 115/5 ( reviews)

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Book Synopsis A Guide to Patient Recruitment by : Diana L. Anderson

Download or read book A Guide to Patient Recruitment written by Diana L. Anderson. This book was released on 2001. Available in PDF, EPUB and Kindle. Book excerpt: A Guide to Patient Recruitment is designed to help clinical research professionals improve the effectiveness of their patient recruitment efforts. Authored by Diana Anderson Ph.D., with contributions from 15 industry leaders, this 350-page guide offers real world, practical recruitment strategies and tactics grounded in facts and experiences. It is an invaluable resource for educating staff on patient recruitment and in managing recruitment initiatives for clinical trials. Developed in accordance with the essentials and standards of the ACCME. Exam is provided online. Topics include... Trends and issues influencing patient recruitment, retention and ethics; Benchmark data on patient volunteer demographics and recruitment costs; Effective media strategies and tactics; Budget considerations; Guidelines on establishing new recruitment and retention practices.

Reinventing Patient Recruitment

2017-03-02 Business & Economics
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Release : 2017-03-02
Genre : Business & Economics
Kind : eBook
Book Rating : 236/5 ( reviews)

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Book Synopsis Reinventing Patient Recruitment by : Joan F. Bachenheimer

Download or read book Reinventing Patient Recruitment written by Joan F. Bachenheimer. This book was released on 2017-03-02. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Global Issues in Patient Recruitment and Retention

2012-01 Clinical trials
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Release : 2012-01
Genre : Clinical trials
Kind : eBook
Book Rating : 634/5 ( reviews)

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Book Synopsis Global Issues in Patient Recruitment and Retention by : Diana L. Anderson-Foster

Download or read book Global Issues in Patient Recruitment and Retention written by Diana L. Anderson-Foster. This book was released on 2012-01. Available in PDF, EPUB and Kindle. Book excerpt: It is well documented that slow patient enrollment is a global contributor of studydelays. Likewise, retaining patients once enrolled can be equally arduous, but just ascritical to the completion and success of a clinical trial. In her second book on thesubject, industry expert Diana Anderson-Foster tackles for the first time the globalchallenges posed by these everyday issues and provides thoughtful analysis and strategicsolutions to minimize recruitment costs and develop successful global patient recruitmentprograms. With insight and contributions from thought-leaders in the industry, this guidealso delves into the sponsor's perspective on patient recruitment and tackles new emergingtopics including technology challenges, phase I recruiting and the role of social media. This guide is a valuable and indispensable resource for anyone involved in clinicaloperations, specifically patient recruitment and retention.

Registries for Evaluating Patient Outcomes

2014-04-01 Medical
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Release : 2014-04-01
Genre : Medical
Kind : eBook
Book Rating : 333/5 ( reviews)

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Book Synopsis Registries for Evaluating Patient Outcomes by : Agency for Healthcare Research and Quality/AHRQ

Download or read book Registries for Evaluating Patient Outcomes written by Agency for Healthcare Research and Quality/AHRQ. This book was released on 2014-04-01. Available in PDF, EPUB and Kindle. Book excerpt: This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.

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