Different interpretation of additional evidence for HTA by the commissioned HTA body and the commissioning decision maker in Germany: whenever IQWiG and Federal Joint Committee disagree
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DOI: 10.1186/s13561-019-0254-6
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References listed on IDEAS
- Niehaus, Ines & Dintsios, Charalabos-Markos, 2018. "Confirmatory versus explorative endpoint analysis: Decision-making on the basis of evidence available from market authorization and early benefit assessment for oncology drugs," Health Policy, Elsevier, vol. 122(6), pages 599-606.
- Maison, Patrick & Zanetti, Laura & Solesse, Anne & Bouvenot, Gilles & Massol, Jacques, 2013. "The public health benefit of medicines: How it has been assessed in France? The principles and results of five years’ experience," Health Policy, Elsevier, vol. 112(3), pages 273-284.
- Fischer, Katharina Elisabeth & Heisser, Thomas & Stargardt, Tom, 2016. "Health benefit assessment of pharmaceuticals: An international comparison of decisions from Germany, England, Scotland and Australia," Health Policy, Elsevier, vol. 120(10), pages 1115-1122.
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More about this item
Keywords
Addenda; AMNOG; IQWiG; Federal Joint Committee; Early benefit assessment; (added benefit; Evidence quality; Agreement statistics);All these keywords.
JEL classification:
- I18 - Health, Education, and Welfare - - Health - - - Government Policy; Regulation; Public Health
Statistics
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