OTCA22 – “Clinical utility of Point-of-care Tests (POCT) D-Dimer and Troponin” project plan and comments from external experts are now available.
EUnetHTA is pleased to announce that the project plan and and comments from external experts for the Other Technologies Collaborative Assessment OTCA22 “Clinical utility of Point-of-care Tests (POCT) D-Dimer and Troponin” are now available for access. The final assessment report will be published on 29th November, 2019. Please access the project plan and external expert […]
PTJA11 – EUnetHTA is pleased to announce the start of the next Pharmaceutical Joint Assessment.
PTJA11 addresses ‘cefiderocol the for the treatment of infections due to aerobic Gram-negative bacteria in adult patients with limited treatment options’, submitted by Shionogi BV. We are delighted that AIFA and NOMA are authoring this assessment. We will be issuing an Open Call for Patient Input in due course.
The public consultation of the revision of the methodological guideline “Process of information retrieval for systematic reviews and health technology assessments on clinical effectiveness” is OPEN (deadline 27th September, 2019)
We are pleased to announce that, as of today, a revised version of the methodological guideline “Process of information retrieval for systematic reviews and health technology assessments on clinical effectiveness”, produced within WP6 B2, has entered the public consultation phase. This consultation will be open until 27th September, 2019. PLEASE NOTE: This was initially 13th […]
PTJA07 Pharmaceutical Joint Assessment Now Available – ustekinumab for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response with, lost response to or were intolerant to either conventional therapy or a biologic or have medical contraindications to such therapies.
This is the pharmaceutical Joint Assessment PTJA07 – on ustekinumab for the treatment of ulcerative colitis (UC). In September 2019, EMA approved the extension of the indication for ustekinumab to include treatment of adult patients with moderately to severely active UC who have had an inadequate response with, lost response to or were intolerant to […]
An Understanding of EUnetHTA HTA
The EUnetHTA Executive Board recently adopted the following Understanding of EUnetHTA HTA. This text is the result of several months of consultation with the project’s board. The EUnetHTA Executive Board agreed that HTA in the context of EUnetHTA activities is understood to be composed of the following elements: Assessments should inform decision-making. Assessments are not decision-making processes themselves. Information should […]
The EUnetHTA Prioritisation List (EPL) 2.0 is now published and available for access
EUnetHTA is pleased to announce the publication of the second iteration of the EPL. As part of the overarching Topic Identitication, Selection and Prioritisation (TISP) task group, the EPL is a valuable strategic tool for companies to identify the significant interest of national HTA bodies in relation to specific listed compounds. EUnetHTA seeks to increase […]
The public consultation of the draft methodological guideline “Practical considerations when critically assessing economic evaluations” is OPEN (deadline Oct. 11, 2019)
We are pleased to announce that, as of today, the draft methodological guideline “Practical considerations when critically assessing economic evaluations”, produced within WP6 B2, has entered the public consultation phase. This consultation will be open until 11th October, 2019. Objective of the methodological guideline EUnetHTA´s methodological guidelines are targeted to the needs of health […]
Public consultation on the guideline ”Process of information retrieval for systematic reviews and health technology assessments on clinical effectiveness” in August/September 2019
The methodological guideline ”Process of information retrieval for systematic reviews and health technology assessments on clinical effectiveness” is currently under revision by IQWiG, NIPHNO and AETSA. It will be made available for public consultation as of beginning of August for the duration of approximately 2 months.
Reminder: Open Call for Patient Input – Joint Assessment on a medicinal product for neovascular (wet) age-related macular degeneration (AMD).
This is a friendly reminder that EUnetHTA recently started a new Joint Assessment on a medicinal product for neovascular (wet) age-related macular degeneration (AMD). To find out about participation, please read more here. Please be advised that input submissions will be received through 13:00, July 15th.
EUnetHTA Magazine – Summer 2019 – Now available
We are pleased to roll out the next issue of EUnetHTA Magazine. As we are now experimenting with a web-based format, we hope to provide a more interactive experience for readers, whether that’s on desktop, tablet, or mobile device. In this issue we have healthcare thoughts from Finland, updates from MD and an interview with […]
