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PRO Data Collection in Clinical Trials Using Mixed Modes
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Indirect Treatment Comparison/Network Meta-Analysis Study Questionnaire to Assess Study Relevance and Credibility to Inform Healthcare Decision-Making - Report 3
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A Questionnaire to Assess the Relevance and Credibility of Observational Studies to Inform Health Care Decision Making - Report 1
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Questionnaire to Assess Relevance and Credibility of Modeling Studies for Informing Health Care Decision Making - Report 2
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Principles of Good Practice for Budget Impact Analysis II
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Performance-Based Risk-Sharing Arrangements - Good Practices for Design, Implementation and Evaluation
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Pediatric Patient-Reported Outcome Instruments for Research to Support Medical Product Labeling
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Validation of Electronic Systems to Collect Patient-Reported Outcome (PRO) Data - Recommendations for Clinical Trial Teams
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Constructing Experimental Designs for Discrete-Choice Experiments
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Prospective Observational Studies to Assess Comparative Effectiveness
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Modeling Good Research Practices - Overview: Report 1
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Conceptualizing a Model: Report 2
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State-Transition Modeling: Report 3
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Modeling Using Discrete Event Simulation: Report 4
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Dynamic Transmission Modeling: Report 5
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Model Parameter Estimation and Uncertainty Analysis: Report 6
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Model Transparency and Validation: Report 7
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Content Validity - Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation Part 1
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Content Validity – Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation Part 2
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Interpreting Indirect Treatment Comparisons and Network Meta-Analysis for Health-Care Decision Making Report 1
- 1
- 2
- 3 (current)
- 4
- 5
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