EUnetHTA 21 Guidance

D4.2: The Scoping Process (PICO)

D4.3.1: Direct and Indirect Comparisons

D4.3.2: Methodological Guideline on Direct and Indirect Comparisons

D4.4: Methodological Guideline on Endpoints

D4.5: Applicability of Evidence – Practical Guideline on Multiplicity, Subgroup, Sensitivity and Post Hoc Analyses

D4.6: Methodological Guidance Regarding the Validity of Clinical Studies

D4.7.1 High Risk Medical devices – Synthesis of national requirements

D4.7.2 Framework for the assessment of high-risk medical devices and in vitro diagnostics

D5.1 JCA Submission Dossier Template

D5.2 JCA Report Template Guidance

D5.3.1: Procedural Guidance for Appointment of Assessors and Co-assessors for JCA/CA

D5.3.2: Resourcing and Maintaining HTAb Technical Expert Working Groups

European Joint Clinical Assessment, EU HTA

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