WP7 SG2 Position paper on how to decide on the appropriate study design for AEG available

WP7 Subgroup 2 is pleased to announce the publication of the Position paper on how to decide on the appropriate study design for primary research arising from HTA reports. This document is one of two WP7 SG2 methodological documents aiming to help HTA authors/systematic reviewers in defining their recommendations for Additional Evidence Generation (AEG). This […]

WP7 SG2 Position paper on how to best formulate research recommendations for AEG

This document is one of two WP7 SG2 methodological documents aiming to help HTA authors/systematic reviewers in defining their recommendations for Additional Evidence Generation (AEG). It is focusing on providing a structured approach for the identification of research gaps and improving the presentation of research recommendations arising from HTA reports. Both uncertainties related to the […]

WP7-SG3 “Therapeutic medical devices” guideline

This guideline on “Therapeutic medical devices”, with answered comments from the SAG / Public consultation, is the last guideline of WP7 Subgroup 3 in JA2. Comments_answers_GL_Ther_medical_devices Therapeutic medical devices_Guideline_Final Nov 2015

WP7 SG2 Core protocol Pilot for AEG available

WP7 Subgroup 2 is pleased to announce the publication of its final deliverable – the Core protocol Pilot for Additional Evidence Generation (AEG). This pilot consists of two parts: – Defining core elements of a study protocol for AEG and developing the template of a Core protocol for AEG (section 1) – Testing the developed […]

WP5 Strand A – Procedure Manual V 4

This document describes processes planned for conducting pilot rapid assessments for pharmaceuticals. Since the Procedure Manual is a living document, further changes can be expected due to experiences gathered throughout JA2. 2012123627 – Procedure_manual_REA pilots_WP5_Strand A

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