My Account Log in

4 options

Sharing clinical research data : workshop summary / Steve Olson and Autumn S. Downey, Rapporteurs, Forum on Drug Discovery, Development, and Translation, Forum on Neuroscience and Nervous System Disorders, National Cancer Policy Forum, Roundtable on Translating Genomic-Based Research for Health, Board on Health Science Policy, Board on Health Care Services, Institute of Medicine of the National Academies.

EBSCOhost Academic eBook Collection (North America) Available online

View online

Ebook Central Academic Complete Available online

View online

NCBI Bookshelf Available online

View online

National Academies Press Available online

View online
Format:
Book
Author/Creator:
Olson, Steve, 1956- author.
Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation, issuing body.
Contributor:
Olson, Steve, 1956- contributor.
Downey, Autumn S., contributor.
Institute of Medicine (U.S.). Forum on Neuroscience and Nervous System Disorders, issuing body.
National Cancer Policy Forum (U.S.), issuing body.
Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health, issuing body.
Institute of Medicine (U.S.). Board on Health Sciences Policy, issuing body.
Institute of Medicine (U.S.). Board on Health Care Services, issuing body.
Language:
English
Subjects (All):
Medical informatics--United States--Congresses.
Medical informatics.
Clinical trials--United States--Congresses.
Clinical trials.
Biology--Research--United States--Congresses.
Biology.
Medicine--Research--United States--Congresses.
Medicine.
Physical Description:
1 online resource (134 p.)
Edition:
1st ed.
Place of Publication:
Washington, District of Columbia : The National Academies Press, [2013]
Language Note:
English
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 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, pre- sent 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.
Contents:
The benefits of data sharing
Barriers to data sharing
Models of data sharing
Standardization to enhance data sharing
Changing the culture of research
Final reflections on sharing clinical research data.
Notes:
Description based upon print version of record.
Includes bibliographical references (pages 81-84).
Description based on print version record.
ISBN:
0-309-26877-X
0-309-26875-3
OCLC:
851693450

The Penn Libraries is committed to describing library materials using current, accurate, and responsible language. If you discover outdated or inaccurate language, please fill out this feedback form to report it and suggest alternative language.

Find

Home Release notes

My Account

Shelf Request an item Bookmarks Fines and fees Settings

Guides

Using the Find catalog Using Articles+ Using your account