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/vufind/Search/Results?lookfor=%22Ruof%2C+J%22&type=Person&sort=year
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PubPharm (79)
1
Review of Relative effectiveness assessments (REAs) of pharmaceuticals at the European network for health technology assessment (EUnetHTA) : A first step towards a consolidated European perspective on comparative effectiveness & safety?
enthalten in:
Health policy (Amsterdam, Netherlands)
| 2020
von
Chassagnol, F.
|
Marcelli, G.
|
Wagle, J.
| +4
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2
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
enthalten in:
Health economics review
| 2019
von
Dintsios, C.
|
Worm, F.
|
Ruof, J.
| +1
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3
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
enthalten in:
Health economics review
| 2019
von
Dintsios, C.
|
Worm, F.
|
Ruof, J.
| +1
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4
Recommendations In Clinical Guidelines, ‘No Benefit’ Ratings, And Opt-Out Decisions In Germany Since The Introduction Of The Amnog Law In 2011: How Do The Pieces Fit Together?
enthalten in:
Value in health
| 2016
von
Staab, T.
|
Dintsios, C.
|
Schulenburg, J.
| +1
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5
Acceptance of Clinically Relevant Primary Study Endpoints In The German Health Technology Assessment Process: Analysis of Five Different Disease Areas
enthalten in:
Value in health
| 2015
von
Isbary, G.
|
Ruof, J.
|
Staab, T.
| +1
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6
G-Ba Does not Adjust Evidence Requirements in Early Benefit Assessment in Cases of Pre-Defined, Efficacy-Based Cross-Over Decisions in Oncology Trials
enthalten in:
Value in health
| 2015
von
Dintsios, C.
|
Isbary, G.
|
Staab, T.
| +2
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7
Comparison of Post-Authorisation Measures From Regulatory Authorities With Additional Evidence Requirements From HTA Bodies in Germany
enthalten in:
Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
| 2014
von
Ruof, J.
|
Staab, T.
|
Slawik, L.
| +2
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8
The Risky Business of Drug Development : The Final Say of National Hta Agencies on A Pharmaceutical's Benefit During The Last Stretch of An Expensive, Long-Lasting And Arduous Development Journey - As Illustrated By The Decisions Of Germany's Gemeinsamer Bundesausschuss (G-Ba)
enthalten in:
Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
| 2014
von
Maetzel, A.
|
Staab, T.
|
Ruof, J.
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9
Dilemma of Cross-Over Trials and Their Impact on Benefit Assessment In Oncology
enthalten in:
Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
| 2014
von
Ruof, J.
|
Staab, T.
|
Walter, M.
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10
Comparison of Post-Authorisation Measures From Regulatory Authorities With Additional Evidence Requirements From HTA Bodies in Germany
enthalten in:
Value in health
| 2014
von
Ruof, J.
|
Staab, T.
|
Slawik, L.
| +2
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Zeitschrift für Rheumatologie
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Thema
32
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Comparative Study
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Antirheumatic Agents
6
Research Support, Non-U.S. Gov't
5
Klinische Studie
5
Multicenter Study
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Randomized Controlled Trial
4
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3
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3
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3
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3
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3
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3
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(added benefit
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Erscheinungszeitraum
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2000-
14
1900-1999
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Englisch
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