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Editorial
. 2020 Oct 30;2(1):e000067.
doi: 10.1136/bmjsit-2020-000067. eCollection 2020.

Authors' response

Affiliations
Editorial

Authors' response

Jack L Cronenwett et al. BMJ Surg Interv Health Technol. .
No abstract available

Keywords: device evaluation; health care costs; real world evidence; vascular devices.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None declared.

References

    1. U.S. Food & Drug Administration, Center for Devices and Radiological Health . Strengthening our national system for medical device Postmarket surveillance: update and next steps, 2018. Available: https://www.fda.gov/media/84409/download [Accessed 5 May 2020].
    1. Wimmer NJ, Robbins S, Ssemaganda H, et al. . Assessing the cost burden of United States FDA-mandated post-approval studies for medical devices. J Health Care Finance 2016;2016. (Spec Features). - PMC - PubMed
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    1. Behrendt CA, Venermo M, Cronenwett JL, et al. . VASCUNET, VQI, and the International Consortium of Vascular Registries - Unique Collaborations for Quality Improvement in Vascular Surgery. Eur J Vasc Endovasc Surg 2019. - PubMed
    1. Particpating centers VQI. Available: https://www.vqi.org/about/vqi-participating-centers/ [Accessed 10 Sep 2020].

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