Non Interventional Studies Europe Part 2
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Non Interventional Studies Europe Part 2
Author | : Anonim |
Publsiher | : CHCUK |
Total Pages | : 322 |
Release | : 2024 |
Genre | : Electronic Book |
ISBN | : 9780956331939 |
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Non Interventional Studies Considerations when Managing and Conducting Non Interventional Studies in Europe Part 2
Author | : Stuart McCully |
Publsiher | : CHCUK |
Total Pages | : 209 |
Release | : 2009 |
Genre | : Clinical trials |
ISBN | : 9780956331915 |
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Non Interventional Studies Europe Part 1
Author | : Anonim |
Publsiher | : CHCUK |
Total Pages | : 190 |
Release | : 2024 |
Genre | : Electronic Book |
ISBN | : 9780956331922 |
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Improving Healthcare Quality in Europe Characteristics Effectiveness and Implementation of Different Strategies
Author | : OECD,World Health Organization |
Publsiher | : OECD Publishing |
Total Pages | : 135 |
Release | : 2019-10-17 |
Genre | : Electronic Book |
ISBN | : 9789264805903 |
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This volume, developed by the Observatory together with OECD, provides an overall conceptual framework for understanding and applying strategies aimed at improving quality of care. Crucially, it summarizes available evidence on different quality strategies and provides recommendations for their implementation. This book is intended to help policy-makers to understand concepts of quality and to support them to evaluate single strategies and combinations of strategies.
Poole s Index to Periodical Literature pt 2 K Z 1802 1881
Author | : William Frederick Poole |
Publsiher | : Unknown |
Total Pages | : 744 |
Release | : 1882 |
Genre | : Periodicals |
ISBN | : UIUC:30112024912567 |
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Registries for Evaluating Patient Outcomes
Author | : Agency for Healthcare Research and Quality/AHRQ |
Publsiher | : Government Printing Office |
Total Pages | : 396 |
Release | : 2014-04-01 |
Genre | : Medical |
ISBN | : 9781587634338 |
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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.
Catalogue of the Library of Parliament
Author | : Canada. Library of Parliament |
Publsiher | : Unknown |
Total Pages | : 826 |
Release | : 1880 |
Genre | : Canada |
ISBN | : UOM:35112105138392 |
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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.