Market competition among manufacturers of novel high-risk therapeutic devices receiving FDA premarket approval between 2001 and 2018

Author:

Rathi Vinay KORCID,Johnston James L,Dhruva SanketORCID,Ross Joseph

Publisher

BMJ

Subject

Biomedical Engineering,Surgery

Reference7 articles.

1. Characteristics of Clinical Studies Conducted Over the Total Product Life Cycle of High-Risk Therapeutic Medical Devices Receiving FDA Premarket Approval in 2010 and 2011

2. Medicare Payment Advisory Commission . Report to the congress: medicare and the health care delivery system. 2017: 207–42. Available: http://www.medpac.gov/docs/default-source/reports/jun17_ch7.pdf?sfvrsn=0

3. Clinical evidence supporting US food and drug administration clearance of novel therapeutic devices via the de novo pathway between 2011 and 2019;Johnston;JAMA Intern Med,2020

4. U.S. Food and Drug Administration . Premarket approval (PMA) database. 2022. Available: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm

5. Competitive development in pharmacologic classes: market entry and the timing of development;DiMasi;Clin Pharmacol Ther,2016

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