EUnetHTA 21 is pleased to announce the publication of three deliverables: D4.3.2 Methodological Guideline on direct and indirect comparisons; D4.7.1/2 Synthesis of national requirements / Framework for the assessment of high-risk medical devices and in-vitro-diagnostics and D5.3.2 Resourcing and maintaining HTAb technical expert working groups (sub deliverable of D5.3).
More information can be found here: https://www.eunethta.eu/jointhtawork/
Many thanks to all involved in the development of the deliverables!
