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Generating Evidence for Genomic Diagnostic Test Development -  Institute of Medicine,  Board on Health Sciences Policy,  Roundtable on Translating Genomic-Based Research for Health

Generating Evidence for Genomic Diagnostic Test Development

Workshop Summary
Buch | Softcover
106 Seiten
2011
National Academies Press (Verlag)
978-0-309-21104-8 (ISBN)
CHF 41,85 inkl. MwSt
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Ten years after the sequencing of the human genome, scientists have developed genetic tests that can predict a person's response to certain drugs, estimate the risk of developing Alzheimer's disease, and make other predictions based on known links between genes and diseases. However, genetic tests have yet to become a routine part of medical care, in part because there is not enough evidence to show they help improve patients' health.


The Institute of Medicine (IOM) held a workshop to explore how researchers can gather better evidence more efficiently on the clinical utility of genetic tests. Generating Evidence for Genomic Diagnostic Test Development compares the evidence that is required for decisions regarding clearance, use, and reimbursement, to the evidence that is currently generated. The report also addresses innovative and efficient ways to generate high-quality evidence, as well as barriers to generating this evidence.


Generating Evidence for Genomic Diagnostic Test Development contains information that will be of great value to regulators and policymakers, payers, health-care providers, researchers, funders, and evidence-based review groups.

Table of Contents


Front Matter
1 Introduction
2 Stakeholder Perspectives on Evidence
3 Approaches to Evidence Generation
4 Overcoming Barriers for Evidence Generation
5 Considerations Moving Forward
6 Final Remarks
References
Appendix A: Workshop Agenda
Appendix B: Speaker Biographical Sketches
Appendix C: Registered Attendees

1 Front Matter; 2 1 Introduction; 3 2 Stakeholder Perspectives on Evidence; 4 3 Approaches to Evidence Generation; 5 4 Overcoming Barriers for Evidence Generation; 6 5 Considerations Moving Forward; 7 6 Final Remarks; 8 References; 9 Appendix A: Workshop Agenda; 10 Appendix B: Speaker Biographical Sketches; 11 Appendix C: Registered Attendees

Verlagsort Washington
Sprache englisch
Maße 152 x 229 mm
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete
Studium 2. Studienabschnitt (Klinik) Anamnese / Körperliche Untersuchung
Studium 2. Studienabschnitt (Klinik) Humangenetik
ISBN-10 0-309-21104-2 / 0309211042
ISBN-13 978-0-309-21104-8 / 9780309211048
Zustand Neuware
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