Read Books Online and Download eBooks, EPub, PDF, Mobi, Kindle, Text Full Free.
A Guide To Patient Recruitment
Download A Guide To Patient Recruitment full books in PDF, epub, and Kindle. Read online A Guide To Patient Recruitment ebook anywhere anytime directly on your device. Fast Download speed and no annoying ads. We cannot guarantee that every ebooks is available!
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.) and published by CenterWatch. This book was released on 2004 with total page 314 pages. 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.
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 and published by CenterWatch. This book was released on 2001 with total page 0 pages. 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.
Book Synopsis Patient Recruitment in Clinical Research by : Danielle Jacobs
Download or read book Patient Recruitment in Clinical Research written by Danielle Jacobs and published by Inst of Clinical Research. This book was released on 2005 with total page 48 pages. Available in PDF, EPUB and Kindle. Book excerpt: Provides ideas for how to improve patient recruitment for clinical trials.
Book Synopsis Reinventing Patient Recruitment by : Joan F. Bachenheimer
Download or read book Reinventing Patient Recruitment written by Joan F. Bachenheimer and published by Routledge. This book was released on 2017-03-02 with total page 278 pages. 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.
Book Synopsis Patient Recruitment in Clinical Trials by : Bert Spilker
Download or read book Patient Recruitment in Clinical Trials written by Bert Spilker and published by Raven Press (ID). This book was released on 1992 with total page 376 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Author :Agency for Healthcare Research and Quality/AHRQ Publisher :Government Printing Office ISBN 13 :1587634333 Total Pages :385 pages Book Rating :4.5/5 (876 download)
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 and published by Government Printing Office. This book was released on 2014-04-01 with total page 385 pages. 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.
Book Synopsis A Practical Guide to Managing Clinical Trials by : JoAnn Pfeiffer
Download or read book A Practical Guide to Managing Clinical Trials written by JoAnn Pfeiffer and published by CRC Press. This book was released on 2017-05-18 with total page 292 pages. Available in PDF, EPUB and Kindle. Book excerpt: A Practical Guide to Managing Clinical Trials is a basic, comprehensive guide to conducting clinical trials. Designed for individuals working in research site operations, this user-friendly reference guides the reader through each step of the clinical trial process from site selection, to site set-up, subject recruitment, study visits, and to study close-out. Topics include staff roles/responsibilities/training, budget and contract review and management, subject study visits, data and document management, event reporting, research ethics, audits and inspections, consent processes, IRB, FDA regulations, and good clinical practices. Each chapter concludes with a review of key points and knowledge application. Unique to this book is "A View from India," a chapter-by-chapter comparison of clinical trial practices in India versus the U.S. Throughout the book and in Chapter 10, readers will glimpse some of the challenges and opportunities in the emerging and growing market of Indian clinical trials.
Book Synopsis Clinical Trials Recruitment Handbook Putting People First by : Leslie Kelly
Download or read book Clinical Trials Recruitment Handbook Putting People First written by Leslie Kelly and published by CreateSpace. This book was released on 2014-12-05 with total page 130 pages. Available in PDF, EPUB and Kindle. Book excerpt: IS THIS GUIDE FOR YOU? This is not a textbook, nor is it a review of the growing literature of in this field. In this guide, we focus on what we know, and clinical lifestyle intervention in an academic research setting (Duke University Medical Center) is what we know best. This is a book of tips, the margin notes from years of trial and error. Much of it will appear as common sense. You will find this book useful if you: - Recruit for lifestyle studies (or other studies) in an academic setting - Study or teach at a technical school or university with a clinical research curriculum - Recruit in clinics, small hospitals, or doctor's offices, where health-care teams take care of study recruitment along with the main business of seeing patients
Book Synopsis Quick Guide to Good Clinical Practice by : Cemal Cingi
Download or read book Quick Guide to Good Clinical Practice written by Cemal Cingi and published by Springer. This book was released on 2016-11-15 with total page 243 pages. Available in PDF, EPUB and Kindle. Book excerpt: This brand-new book offers a reference guide to understanding and applying the rules for properly conducting clinical trials to meet the international quality standard – Good Clinical Practice – provided by the International Conference on Harmonization (ICH). The work offers an updated perspective on the clinical research landscape within the context of the clinical trial regulatory frameworks in Europe and the USA. In addition to providing a historical review and a detailed definition of GPC regulations, it includes step-by-step explanations of all the requirements that researchers should bear in mind when designing and performing new trials. Further topics covered include: ethics of clinical research; the drug development process and evolution of regulations; investigator and sponsor responsibilities; and clinical trial protocols. Written by clinicians for clinicians, the book represents a valuable read also for researchers, pharmacists and all professionals involved in applications to the ethic committees, whose approval is required for new clinical studies.
Book Synopsis Accelerating Patient Recruitment in Clinical Trials by :
Download or read book Accelerating Patient Recruitment in Clinical Trials written by and published by NetworkPharma Ltd. This book was released on 2006 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Sharing Clinical Trial Data by : Institute of Medicine
Download or read book Sharing Clinical Trial Data written by Institute of Medicine and published by National Academies Press. This book was released on 2015-04-20 with total page 236 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Book Synopsis Transforming Clinical Research in the United States by : Institute of Medicine
Download or read book Transforming Clinical Research in the United States written by Institute of Medicine and published by National Academies Press. This book was released on 2010-10-22 with total page 151 pages. Available in PDF, EPUB and Kindle. Book excerpt: An ideal health care system relies on efficiently generating timely, accurate evidence to deliver on its promise of diminishing the divide between clinical practice and research. There are growing indications, however, that the current health care system and the clinical research that guides medical decisions in the United States falls far short of this vision. The process of generating medical evidence through clinical trials in the United States is expensive and lengthy, includes a number of regulatory hurdles, and is based on a limited infrastructure. The link between clinical research and medical progress is also frequently misunderstood or unsupported by both patients and providers. The focus of clinical research changes as diseases emerge and new treatments create cures for old conditions. As diseases evolve, the ultimate goal remains to speed new and improved medical treatments to patients throughout the world. To keep pace with rapidly changing health care demands, clinical research resources need to be organized and on hand to address the numerous health care questions that continually emerge. Improving the overall capacity of the clinical research enterprise will depend on ensuring that there is an adequate infrastructure in place to support the investigators who conduct research, the patients with real diseases who volunteer to participate in experimental research, and the institutions that organize and carry out the trials. To address these issues and better understand the current state of clinical research in the United States, the Institute of Medicine's (IOM) Forum on Drug Discovery, Development, and Translation held a 2-day workshop entitled Transforming Clinical Research in the United States. The workshop, summarized in this volume, laid the foundation for a broader initiative of the Forum addressing different aspects of clinical research. Future Forum plans include further examining regulatory, administrative, and structural barriers to the effective conduct of clinical research; developing a vision for a stable, continuously funded clinical research infrastructure in the United States; and considering strategies and collaborative activities to facilitate more robust public engagement in the clinical research enterprise.
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 and published by . This book was released on 2012-01 with total page 262 pages. 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.
Author :National Health and Medical Research Council (Australia) Publisher : ISBN 13 :9780648464426 Total Pages :0 pages Book Rating :4.4/5 (644 download)
Book Synopsis National Statement on Ethical Conduct in Human Research 2023 by : National Health and Medical Research Council (Australia)
Download or read book National Statement on Ethical Conduct in Human Research 2023 written by National Health and Medical Research Council (Australia) and published by . This book was released on 2023 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: "The purpose of the National Statement is to promote ethically good human research. Fulfilment of this purpose requires that participants be accorded the respect and protection that is due to them. It also involves the fostering of research that is of benefit to the community. The National Statement is therefore designed to clarify the responsibilities of: institutions and researchers for the ethical design, conduct and dissemination of results of human research ; and review bodies in the ethics review of research. The National Statement will help them to meet their responsibilities: to identify issues of ethics that arise in the design, review and conduct of human research, to deliberate about those ethical issues, and to justify decisions about them"--Page 6.
Author :Penny M. Crow Publisher :Medical Group Management Association/Center for Research in Ambulatory Health Care Administration ISBN 13 :9781568296821 Total Pages : pages Book Rating :4.2/5 (968 download)
Book Synopsis The Simple Guide to Patient Access Hiring by : Penny M. Crow
Download or read book The Simple Guide to Patient Access Hiring written by Penny M. Crow and published by Medical Group Management Association/Center for Research in Ambulatory Health Care Administration. This book was released on 2019 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: "This Simple Guide provides detailed information on Patient Access Positions, the positions that are key to getting your patients through the door of your medical practice while creating a memorable experience during their visit. This is written for anyone who has a hand in the hiring and recruitment process"--
Book Synopsis Clinical Trials and Human Research by : Fay A. Rozovsky
Download or read book Clinical Trials and Human Research written by Fay A. Rozovsky and published by Jossey-Bass. This book was released on 2003-06-10 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This easy-to-read reference book provides a practical approach for dealing with the legal and regulatory compliance issues involved in human research. Covering a broad range of topics, such as consent, confidentiality, subject recruitment and selection, the role of the investigator and Institutional Review Board, it offers timely and useful strategies for achieving regulatory compliance while reducing liability. In addition, insurance, quality management, accreditation, and risk management are topics examined in the book. The practical insights found in this volume are not found in other books on the subject. Clinical Trials and Human Research is a practical tool to help anyone involved in clinical research.
Book Synopsis Clinical Trial Manager - The Comprehensive Guide by : Viruti Shivan
Download or read book Clinical Trial Manager - The Comprehensive Guide written by Viruti Shivan and published by Viruti Shivan. This book was released on 2024-04 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Mastering the Art of Effective Clinical Research Management for Breakthrough Success In an era where the pace of medical innovation is faster than ever, "Clinical Trial Manager - The Comprehensive Guide" emerges as an indispensable resource for professionals navigating the complex landscape of clinical research management. This book serves as a beacon, guiding readers through the intricacies of planning, executing, and overseeing clinical trials with precision and ethical rigor. By emphasizing a strategic approach that melds scientific insight with managerial acumen, it prepares readers to spearhead research projects that can transform patient care and advance medical knowledge. Its unique appeal lies in the synthesis of expert knowledge with practical, actionable strategies, ensuring readers are well-equipped to tackle contemporary challenges in the field. Notably, this guide is crafted without the inclusion of images or illustrations, a deliberate choice to focus on the richness of content and avoid copyright issues, thus ensuring that its wisdom is accessible and unencumbered by such constraints. Diving deeper, "Clinical Trial Manager - The Comprehensive Guide" not only demystifies the regulatory landscape shaping clinical research but also illuminates the path to effective team leadership and stakeholder engagement. Readers will discover a treasure trove of insights into data management, patient recruitment strategies, and the nuances of global trials, all woven together with real-world examples and hypothetical scenarios. These narratives not only embellish the text with a layer of relatability but also serve as a catalyst for imagination, pushing readers to envision themselves at the helm of groundbreaking trials. As such, this book stands out as a must-buy for aspiring and seasoned professionals alike, promising to enrich their journey towards becoming pivotal contributors to the field of clinical research.
