Core Resources For Clinical Research
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Core Resources for Clinical Research
Author | : Helena Korjonen-Close |
Publsiher | : Inst of Clinical Research |
Total Pages | : 48 |
Release | : 2007 |
Genre | : Medicine |
ISBN | : 9781905238446 |
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Transforming Clinical Research in the United States
Author | : Institute of Medicine,Board on Health Sciences Policy,Forum on Drug Discovery, Development, and Translation |
Publsiher | : National Academies Press |
Total Pages | : 151 |
Release | : 2010-10-22 |
Genre | : Medical |
ISBN | : 9780309163354 |
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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.
NIH Guide for Grants and Contracts
Author | : National Institutes of Health (U.S.) |
Publsiher | : Unknown |
Total Pages | : 580 |
Release | : 1989 |
Genre | : Research grants |
ISBN | : STANFORD:36105219414641 |
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Research Awards Index
Author | : Anonim |
Publsiher | : Unknown |
Total Pages | : 776 |
Release | : 1989 |
Genre | : Medicine |
ISBN | : UOM:39015014022589 |
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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.
Biomedical Index to PHS supported Research
Author | : Anonim |
Publsiher | : Unknown |
Total Pages | : 866 |
Release | : 1990 |
Genre | : Medicine |
ISBN | : UOM:39015072175162 |
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Vision Research The 1983 report of the National Eye Council
Author | : Anonim |
Publsiher | : Unknown |
Total Pages | : 112 |
Release | : 1983 |
Genre | : Eye |
ISBN | : MINN:30000010684920 |
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Departments of Labor and Health Education and Welfare appropriations for 1980
Author | : United States. Congress. House. Committee on Appropriations. Subcommittee on the Departments of Labor and Health, Education, and Welfare |
Publsiher | : Unknown |
Total Pages | : 1728 |
Release | : 1979 |
Genre | : Electronic Book |
ISBN | : UOM:39015081270616 |
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