Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Steve Olson and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies.

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Material type: Text

text

Media type:

computer

Carrier type:

online resource

ISBN:

9780309253949
0309253942
9780309253956
0309253950
1283636298
9781283636292
0309253977
9780309253970

Subject(s): Genre/Form:

Additional physical formats: Print version:: No titleDDC classification:

576.5 22

LOC classification:

RB155.6 .G46 2012eb

NLM classification:

2012 I-713
QZ 52

Online resources:

Click here to access online

Contents:

Introduction -- Calls for Change -- Test Developers -- Patients -- Payers -- Regulation, Reimbursement, and Public Health -- Discussion of Major Proposals -- References -- Appendix A: Workshop Agenda -- Appendix B: Speaker Biographical Sketches -- Appendix C: Statement of Task -- Appendix D: Registered Attendees.

Abstract: The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guideline inclusion, coverage, and reimbursement of genomic diagnostic tests among stakeholders with the goal of clarifying a pathway for successfully bringing tests to clinical use for the benefit of patients. Presenters at the workshop were asked to consider four broad issues:1. How are the barriers to successful genomic test development viewed?2. What are potential solutions?3. What are the obstacles to achieving those solutions?4. How can those obstacles be overcome?

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Includes bibliographical references.

The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guideline inclusion, coverage, and reimbursement of genomic diagnostic tests among stakeholders with the goal of clarifying a pathway for successfully bringing tests to clinical use for the benefit of patients. Presenters at the workshop were asked to consider four broad issues:1. How are the barriers to successful genomic test development viewed?2. What are potential solutions?3. What are the obstacles to achieving those solutions?4. How can those obstacles be overcome?