EUnetHTA published report with overview of HTA and reimbursement process in 31 EUnetHTA partner countries

31

Jan 2018

In the beginning of December, the European Network of Health Technology Assessment (EUnetHTA) performed evaluation of reimbursement and HTA process in 31 EUnetHTA partner countries. The aim of the study was to improve HTA cooperation between countries, use jointly produced HTA information and re-use national, regional HTA information.

For this purpose HTA agencies and decision-makers who use HTA information were asked by EUnetHTA to provide description of HTA and reimbursement of pharmaceutical and non-pharmaceutical health technologies in outpatient and inpatients settings.

In results, data for analysis were received from 59 agencies. Information was extracted into Excel tables and gathered in following topics:

  • Description of HTA process
  • Horizon scanning and topic selection
  • Description of HTA assessment process
  • Advice and decision making
  • Legal and procedural issues
  • Reassessment
  • Stakeholder involvement

Additionally, EUnetHTA analyzed restrictions regarding type of technology for assessment, timelines for procedures, number of topics for assessment, types (single technology assessment, multiple technology assessment) and approaches (relative effectiveness assessment, clinical effectiveness, economical analyses and full HTA) of initial assessment of health technologies in majority of European countries.

See full report in English here

Subscribe to our newsletter delivered every second week not to miss important reimbursement information.

The latest related news

24

Mar 2022

The HTA body of the Tuscany Regional Healthcare issues two types of documents: HTA forms and motivational forms. With a regional decree 2472 of February 10, 2022, Tuscany Regional Healthcare has published assessments of five medical devices of various therapeutic areas, such as cardiovascular and peripheral vascular areas.

Read more

18

Mar 2022

On February 22, 2022, a repository of innovative acts outside the nomenclature of biology and anatomopathology (RIHN) and a Supplementary list of IVD tests were published. Minor changes were introduced in the 2022 RIHN list.

Read more

15

Mar 2022

The Belgian Health Care Knowledge Center (KCE) initiated a study aimed at defining a clear and transparent procedure for the evaluation of digital health technologies in Belgium.

Read more

14

Mar 2022

In February 2021, the Clinical Coding and Schedule Development (CCSD) working group, which develops and maintains procedural and diagnostics nomenclature for private payers in England, published Bulletins 0182 and 0079 with changes to be implemented no later than April 10, 2022. Three new procedure codes concerned robotic surgery in orthopaedic area, spinal procedures, and ophthalmology, and five new diagnostic codes were introduced.

Read more

11

Mar 2022

On February 07, 2022, the Dental and Pharmaceutical Benefits Agency has announced the withdrawal of the assessments of the PhysioMem PM 100 and CardioMem CM 100 XT and the finalization of the assessments of the Zenicor ECG, Coala Heart Monitor Pro, and KardiaMobile. For the conducted assessments, it was outlined that the portable devices provide more limited information than standard ECG measurements; therefore, it was mainly estimated for atrial fibrillation.

Read more