News
Statement on the Joint Action 3 Prolongation
EUnetHTA Joint Action 3 has received official approval from Consumers, Health, Agriculture and Food Executive Agency (CHAFEA) for an extension of an additional 12 months
EUnetHTA 2020 Assembly – Welcome Guide now available
The annual EUnetHTA Assembly aims to provide an overview into the year’s activity, while stimulating discussion on HTA-related topics and looking to the network’s next
EUnetHTA Response to COVID-19
We all are faced with an unprecedented situation, a reminder of how fragile we as individuals are, how fragile our societies remain. EUnetHTA is a
PTJA09 – Brolucizumab for the treatment of adults with neovascular (wet) age-related macular degeneration (AMD)
This is the pharmaceutical Joint Assessment PTJA09 on brolucizumab. In February 2020, the European Commission granted marketing authorisation for Beovu® (brolucizumab) for the treatment of
EUnetHTA releases a new guidance document that supports health technology assessments: “Practical considerations when critically assessing economic evaluations”
The aim of this guidance document is to pass on some knowledge and know-how to all stakeholders with an interest in economic evaluations by providing
Statement from the EUnetHTA Secretariat on COVID-19
Due to the developing COVID-19 scenario affecting Europe and with regard to the policy responses emerging on a per national basis from certain areas, the
1st Collaborative Assessment – Wearable cardioverter-defibrillator (WCD) therapy in primary and secondary prevention of sudden cardiac arrest in patients at risk
Sudden cardiac arrest (SCA) is the most common cause of death in patients with coronary artery disease. Mostly, ventricular tachycardia and ventricular fibrillation are the
PTJA08 – Siponimod for the treatment of adult patients with secondary progressive multiple sclerosis (SPMS) with active disease evidenced by relapses or imaging features of inflammatory activity
This is the pharmaceutical Joint Assessment PTJA08 – on siponimod for the treatment of active SPMS. In January 2020, the European Commission granted marketing authorisation
PTJA06 – Polatuzumab vedotin in combination with bendamustine and rituximab for the treatment of relapsed/refractory diffuse large B-cell lymphoma (DLBCL) who are not candidates for haematopoietic stem cell transplant
This is the pharmaceutical Joint Assessment PTJA06 – on polatuzumab vedotin for the treatment of relapsed/refractory DLBCL. In January 2020, The European Commission granted conditional
EUnetHTA Magazine – Winter 2020 – Now Available
We are pleased to publish the Winter 2020 issue of EUnetHTA Magazine, our quarterly update on HTA with input from network stakeholders. As always, we
