The EUnetHTA Submission Template is a flexible tool that reflects all national evidence requirements for reimbursement in Europe. The inclusion of all national requirements means that the template can be broadly applied to national and/or joint assessment. The adaptation process must include tailoring the tool’s content to either national HTA processes or joint processes to reflect the methodology adopted and the assessment process of the HTA agency or agencies involved.
Such flexibility of the template allows the HTA agencies to – according to national needs – add, remove and adapt questions and provide further information to aid completion of the template by the technology developers that are required to submit evidence in support of their technology’s value claims. A set of adaptation notes have been created to support HTA agencies with the adaptation process.
EUnetHTA evidence submission template for medical devices long form
EUnetHTA evidence submission template for medical devices short form
EUnetHTA evidence submission template for pharmaceuticals long form
EUnetHTA evidence submission template for pharmaceuticals short form
EUnetHTA evidence submission templates adaptation notes for agencies
Report on evidence requirements for pharmaceuticals and medical devices across Europe
