The EUnetHTA evidence submission template was developed from an analysis of evidence requirements for reimbursement in Europe. It is a tool that agencies can use to request evidence from companies to support their HTA and reimbursement processes. The tool covers relative effectiveness assessment including a description of the health condition and health technology, as well as clinical effectiveness and safety information. It also includes requests for information about the methodology used to produce the HTA (for example how studies were identified). Versions are available for pharmaceuticals and medical devices.
EUnetHTA evidence submission template_pharma_long FINAL3_docxversion
EUnetHTA evidence submission template_pharma_short FINAL3_docxversion
EUnetHTA narrative report evidence requirements_FINAL2
EUnetHTA evidence submission template_adaptation notes FINAL2
EUnetHTA evidence submission template_meddev_long FINAL3_docxversion
EUnetHTA evidence submission template_medev_short FINAL3_docxversion