Regulation of health-related technologies in Germany
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- 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:
- 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.
- 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.
- 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.
- 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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