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The ongoing implementation of healthcare reform policies is leading many medical device companies to rethink their strategies for product innovation, and could lead to the flight of capital and companies to other countries, according to panelists at InHealth’s 2011 Health Technology Summit, held recently in Washington, DC.
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Amid cautious optimism for opportunities still to come as a result of healthcare reform, panelists focused on the central theme of the summit, “Healthcare Reform at Year One: Will More Policy Mean Less Technology?“ The annual Health Technology Summit is a cornerstone of InHealth’s educational programs, which convene key stakeholders––including policymakers, payers, clinicians, providers, and industry executives––to advance understanding about the role of medical technology innovation in society, the economy, and people’s lives.
How well U.S. leadership in medtech innovation will weather the next wave of reform may depend on how future rules and regulations address the healthcare system’s complexity, whether medtech companies can adapt to meet increasing evidence requirements of multiple industry stakeholders, and whether investors will continue to supply the funding needed to develop innovative, effective products. Summit panelists identified a number of factors that will shape the reform-era pipeline for medical technologies:
“This summit challenged panelists to assess how present and future versions of healthcare reform policies will affect the pipeline for medical technology innovation,” said Martyn Howgill, InHealth’s executive director. “Answering this question should be a top priority, as it will have widespread repercussions for the economy and patients alike.”
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Welcome
and Introductions
Martyn
W. C. Howgill
Executive Director
Institute for Health Technology Studies
Robert
J. Rubin, MD
Conference Chair
Clinical Professor of Medicine, Georgetown University
Member, InHealth Board of Directors
Chair, InHealth Research Council
Keynote
Medical
Technology in the Era of Reform
David
M. Cutler, PhD, Dean of Social Science, Harvard
University
In this keynote presentation, healthcare economist and
national policy advisor David Cutler explores how policies and practices
brought about by healthcare reform may stimulate or impede investment,
development, adoption, or use of medical technologies—and how medtech
companies and policymakers can best respond in order to preserve patient
access to those technologies.
Session 1
The Changing Environment for
Demonstrating What Works in Healthcare
Moderator:
Clifford Goodman, PhD,
Senior Vice President and Principal, The Lewin Group; Chair, MEDCAC
Creation of the Patient-Centered Outcomes Research Institute
(PCORI) accompanies changing evidence expectations for validating
medical technologies in the United States and globally. In this session,
researchers discuss how PCORI will interact with such agencies as AHRQ,
CMS, FDA, and NIH as well as other public- and private-sector
organizations, and implications for the medtech sector.
Panelists include:
Bonnie
Handke, RN, MBA
Senior Director for Reimbursement
Neuromodulation Division, Medtronic Inc.
Mark
Helfand, MD, MS, MPH
Professor of Medicine, Professor of Medical Informatics and Clinical
Epidemiology
Director, Evidence-Based Practice Center, Oregon Health and Sciences
University
Jeffrey
C. Lerner, PhD
President and CEO
ECRI Institute
Harlan
F. Weisman, MD
Chief Science and Technology Officer
Medical Devices and Diagnostics Group, Johnson & Johnson
Morning Break Sponsored by Latham & Watkins
Session 2
Payer Innovation and Access to
Healthcare Technology
Moderator:
Leslie V. Norwalk, JD,
Strategic Counsel, Epstein Becker & Green
The new CMS Innovation Center is charged with developing and diffusing
new care and payment models to improve the Medicare and Medicaid
programs, and benefit the healthcare system. But while guiding
experiments with accountable care organizations, health home and medical
home concepts, bundled payment systems, and more, can the center
preserve access to advanced medical technologies? In this session,
experts discuss medtech's prospects in the context of future reforms.
Panelists include:
Kenneth
Barrette
Principal
Optimity Advisors
Liesl
Cooper, PhD
Vice President for Global Healthcare Economics, Policy, and
Reimbursement
Covidien
Ted
Epperly, MD
Program Director and Chief Executive Officer
Family Medicine Residency of Idaho
Luncheon and Executive Interview
Medtech, Innovation, and the ‘New Normal’
Moderator:
Stuart S. Kurlander, MHA, JD,
Senior Partner, Health Care and Life Sciences Practice, Latham &
Watkins LLP
In this moderated interview, experts from the provider community discuss
how their institutions are handling the emerging opportunities to
implement healthcare innovations, and what their changes will mean for
the adoption and use of advanced medical technologies. Featured speakers
for this special session:
Carol
Harding
Senior Director
Supply Chain Innovations and Organizational Transformation The Cleveland
Clinic
Craig
E. Samitt, MD, MBA
President and CEO
Dean Health Systems
Session 3
Reform, Investment, and
Innovation
Moderator:
Gregory de Lissovoy, PhD,
MPH, Adjunct Associate Professor, Johns Hopkins Bloomberg School of
Public Health
Healthcare reform remains a work in progress, with many
programs still to be developed, many policies still in flux, and
significant changes to the legislation still a possibility. In this
session medtech investors and business development professionals
consider the impact of such uncertainties on the current and future
pipeline for medtech innovation. Panelists for the session
include:
Allan
W. May
Founder and Chairman, Life Science Angels
Chair, Angel Capital Education Foundation
Susan
E. Morano, MBA
Worldwide Vice President for New Business Development
Medical Devices and Diagnostics Group, Johnson & Johnson
Kelly
Campbell Slone
Director, Medical Industry Group
National Venture Capital Association
Adjournment
Martyn W. C. Howgill
Institute for Health Technology Studies
Sponsorship provided by: