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look back at 2008
  • 100+ participants
  • 8 health agency speakers
  • 21 sessions over 3 days
  • 65% industry participation
  • 28 hours total duration
  • 7 hours networking time
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    conference details
    Conference:
    Pre-conference workshop
    8 December 9am - 5pm
    Day 1
    9 December 8am - 5.30pm
    Day 2
    10 December 8am - 5.30pm
    Post-conference workshop
    11 December 9am - 5pm
     
    Venue: Royal Garden Hotel, London, United Kingdom
     
     
    Register online now 
    or call +44 (0) 207 608 7055

     

     

     

    Dr Gepke Delwel

    Dr Gepke Delwel,
    Senior Policy Advisor
    College voor Zorgverzekeringen

    Gepke Delwel studied BioMedical Sciences (Faculty of Medicine, State University of Leiden). She holds a PhD for her research on cell adhesion molecules in the Netherlands Cancer Institute (Amsterdam). After her PhD research she got involved in Pharmaco-economics. As a consultant for The Lewin Group she worked on international pharmaco-economic studies and disease management programmes for a number of pharmaceutical companies. In 2000 she joined the Health Care Insurance Board as a policy advisor on pharmaco-economics. She was involved in the implementation of pharmaco-economics in the appraisal procedure for the reimbursement of new drugs. The first experiences with the appraisal of pharmaco-economic studies have been evaluated and the guidelines for pharmaco-economic research, the costing manual and the appraisal procedure were revised. From January 1st 2005 pharmaco-economic studies are obligatory for the reimbursement of new drugs. She is involved in the technical appraisal of these studies. In 2006 the Health Care Insurance Board started with the appraisal of expensive hospital drugs. Part of the appraisal process is outcomes research on clinical, economic and patient reported outcomes of these drugs. Currently, her focus is the implementation and technical requirements of outcomes research in the appraisal process of hospital drugs.
    Appearing:
    Day One – Wednesday 9 December 2009
    3.50pm

    HTA in the Netherlands

    • The role of HTA in coverage decisions: assessment and appraisal in the Netherlands
    • The role of the cost-effectiveness criterium in the reimbursement of extramural drugs based on an evaluation of submissions from 2005 onwards.
    • Latest developments on conditional reimbursement 'CED' for hospital based drugs: guidance for outcomes research and the decisions process based on results of outcomes research
    Senior Policy Advisor,
    College voor Zorgverzekeringen

    Sponsors
     

     
    our speakers
    Meindert Boysen
    Associate Director Single Technology Appraisals
    NICE
     
    Dr François Meyer
    Director, Health Technology Assessment Division
    Haute Autorité de
    Santé
     
    Dr Allan Korn
    Senior Vice President, Chief Medical Officer
    BlueCross BlueShield Association
     
    Jerome Boehm
    Head EU level activities on HTA
    European Commission
     
    Dr Matthias Perleth
    Head of Methods Department
    Gemeinsamer Bundesausschuss

     

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