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Regulation of health-related technologies in Germany

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  • Perleth, Matthias
  • Busse, Reinhard
  • Schwartz, Friedrich Wilhelm

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  • Perleth, Matthias & Busse, Reinhard & Schwartz, Friedrich Wilhelm, 1999. "Regulation of health-related technologies in Germany," Health Policy, Elsevier, vol. 46(2), pages 105-126, January.
    • Handle: RePEc:eee:hepoli:v:46:y:1999:i:2:p:105-126
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    References listed on IDEAS

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    1. Kirchberger, Stefan, 1994. "Health care technology in the Federal Republic of Germany," Health Policy, Elsevier, vol. 30(1-3), pages 163-205.
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    Cited by:

    1. Fuchs, Sabine & Olberg, Britta & Perleth, Matthias & Busse, Reinhard & Panteli, Dimitra, 2019. "Testing a new taxonomic model for the assessment of medical devices: Is it plausible and applicable? Insights from HTA reports and interviews with HTA institutions in Europe," Health Policy, Elsevier, vol. 123(2), pages 173-181.
    2. Walshe, Ronald & Schmitz, Norbert & Diehl, Volker, 1999. "Can corporatization contribute to quality assurance and cost control in the German hospital sector?: A pilot project for stem cell transplantation," Health Policy, Elsevier, vol. 48(3), pages 207-218, August.
    3. Zippel, Claus & Bohnet-Joschko, Sabine, 2017. "Post market surveillance in the german medical device sector – current state and future perspectives," Health Policy, Elsevier, vol. 121(8), pages 880-886.
    4. Schreyögg, Jonas & Henke, Klaus-Dirk & Busse, Reinhard, 2004. "Managing pharmaceutical regulation in Germany: Overview and economic assessment," Discussion Papers 2004/6, Technische Universität Berlin, School of Economics and Management.

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    1. Rembrandt D. Scholz & Sebastian Klüsener, 2012. "Regional hot spots of exceptional longevity in Germany," MPIDR Working Papers WP-2012-028, Max Planck Institute for Demographic Research, Rostock, Germany.

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