Monday, 26 October 2009
7:00-8:00
Comparative Effectiveness: Can the Agencies’ Demands Be Met?
As decision-makers and the citizens they serve demand stronger evidence to support coverage, prioritization, and pricing, the need for comparative effectiveness research has come to the fore. Traditional clinical trial designs provide valid data but are extremely expensive and time consuming, making them not very practical. Even if everybody agrees that better information on relative effectiveness is required for improving the quality of health care decisions, the entities involved have not identified a common approach to this new challenge.
This symposium will explore the views of three major agencies (NICE, HAS and IQWiG) involved in evaluating new products on the requirements for this type of data. What methods will they find acceptable? Which ones not? How soon does the information need to be available? Who can collect it? Who should collect it? What about funding? What is the role of various stakeholders? What changes are expected? Is simulation the solution? Is it possible to develop a unified approach? Is it desirable? We will open up the symposium for discussion of the advantages of various methods, the challenges, the future trends and possible implications.
Moderator:
J. Jaime Caro MDCM, FRCPC, FACP, Senior Vice-President of Health Economics, United BioSource Corporation, Lexington, MA, USA
Speakers:
Kalipso Chalkidou MD, PhD, Director, National Institute for Health and Clinical Excellence (NICE), London, UK
Andreas Gerber MD, PhD, MA, MSc, Head of Health Economics Department, Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG), Cologne, Germany
Claire Le Jeunne MD, PhD, Vice President, Haute Autorité de Santé (HAS), Paris, France
Sponsored by UBC and Shire