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How Can Health Technology Assessments in the Asia-Pacific Area Respond to Increased Clinical Uncertainty as a Consequence of Expedited US and EU Regulatory Processes?

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  • Amanda Cole;Adrian Towse;Michelle Mujoomdar;Arnold Chan;Franz Pichler

Abstract

This report provides a detailed summary of a panel session which took place at the HTAi 2016 annual meeting, Tokyo. The panel session was entitled "How Can HTA in Asia-Pacific Respond to Increased Clinical Uncertainty as a Consequence of Expedited US and EU Regulatory Processes?" and was chaired by Franz Pichler (Eli Lilly & Company).

Suggested Citation

  • Amanda Cole;Adrian Towse;Michelle Mujoomdar;Arnold Chan;Franz Pichler, 2016. "How Can Health Technology Assessments in the Asia-Pacific Area Respond to Increased Clinical Uncertainty as a Consequence of Expedited US and EU Regulatory Processes?," Briefing 001740, Office of Health Economics.
    • Handle: RePEc:ohe:briefg:001740
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    File URL: https://www.ohe.org/publications/how-can-health-technology-assessments-asia-pacific-area-respond-increased-clinical/attachment-htai-panel-session-uncertainty-august-2016/
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    Keywords

    How Can Health Technology Assessments in the Asia-Pacific Area Respond to Increased Clinical Uncertainty as a Consequence of Expedited US and EU Regulatory Processes?;

    JEL classification:

    • I1 - Health, Education, and Welfare - - Health

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