Are Medical Device Characteristics Included in HTA Methods Guidelines and Reports? A Brief Review
Author:
Funder
Medtronic
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40258-024-00896-y.pdf
Reference39 articles.
1. Health technology assessment of medical devices WHO. Medical device technical series. Geneva: World Health Organization; 2011.
2. Chamova J. Mapping of HTA national organisations, programmes and processes in EU and Norway. Brussels: European Commission; 2017.
3. Fuchs S, et al. Health technology assessment of medical devices in europe: processes, practices, and methods. Int J Technol Assess Health Care. 2016;32(4):246–55.
4. Ciani O, et al. Linking the regulatory and reimbursement processes for medical devices: the need for integrated assessments. Health Econ. 2017;26(Suppl 1):13–29.
5. Bluher M, et al. Critical review of European health-economic guidelines for the health technology assessment of medical devices. Front Med (Lausanne). 2019;6:278.
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