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Sharing clinical research data : workshop summary /

Pharmaceutical companies, academic researchers, and government agencies such as the Food and Drug Administration and the National Institutes of Health all possess large quantities of clinical research data. If these data were shared more widely within and across sectors, the resulting research advan...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores principales: Olson, Steve, 1956- (Autor), Downey, Autumn S. (Autor)
Autores Corporativos: Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation (sponsoring body.), Institute of Medicine (U.S.). Forum on Neuroscience and Nervous System Disorders (sponsoring body.), National Cancer Policy Forum (U.S.) (sponsoring body.), Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health (sponsoring body.), Sharing Clinical Research Data (Workshop)
Formato: Electrónico Congresos, conferencias eBook
Idioma:Inglés
Publicado: Washington, D.C. : The National Academies Press, [2013]
Temas:
Acceso en línea:Texto completo
Descripción
Sumario:Pharmaceutical companies, academic researchers, and government agencies such as the Food and Drug Administration and the National Institutes of Health all possess large quantities of clinical research data. If these data were shared more widely within and across sectors, the resulting research advances derived from data pooling and analysis could improve public health, enhance patient safety, and spur drug development. Data sharing can also increase public trust in clinical trials and conclusions derived from them by lending transparency to the clinical research process. Much of this information, however, is never shared. Retention of clinical research data by investigators and within organizations may represent lost opportunities in biomedical research. Despite the potential benefits that could be accrued from pooling and analysis of shared data, barriers to data sharing faced by researchers in industry include concerns about data mining, erroneous secondary analyses of data, and unwarranted litigation, as well as a desire to protect confidential commercial information. Academic partners face significant cultural barriers to sharing data and participating in longer term collaborative efforts that stem from a desire to protect intellectual autonomy and a career advancement system built on priority of publication and citation requirements. Some barriers, like the need to protect patient privacy, present challenges for both sectors. Looking ahead, there are also a number of technical challenges to be faced in analyzing potentially large and heterogeneous datasets. This public workshop focused on strategies to facilitate sharing of clinical research data in order to advance scientific knowledge and public health. While the workshop focused on sharing of data from preplanned interventional studies of human subjects, models and projects involving sharing of other clinical data types were considered to the extent that they provided lessons learned and best practices. The workshop objectives were to examine the benefits of sharing of clinical research data from all sectors and among these sectors, including, for example: benefits to the research and development enterprise and benefits to the analysis of safety and efficacy. Sharing Clinical Research Data: Workshop Summary identifies barriers and challenges to sharing clinical research data, explores strategies to address these barriers and challenges, including identifying priority actions and "low-hanging fruit" opportunities, and discusses strategies for using these potentially large datasets to facilitate scientific and public health advances.
Notas:Title from PDF title page.
Descripción Física:1 online resource (1 PDF file (xxii, 134 pages))
Bibliografía:Includes bibliographical references.
ISBN:9780309268745
0309268745
9780309268752
0309268753