Alam, M., Shi, V. J., Maisel-Campbell, A., Cressey, B. D., Nadir, U., Koza, E., Haq, M., Ahmed, A., Ma, M. S., Weil, A., Cahn, B. A., Lee, A. Y., Shapiro, S., & Poon, E. (2024). US FDA Advisory Panel Members’ Assessment of Premarket Approval Process and Suggestions for Improvement. JAMA Network Open, 7(10), e2436066. https://doi.org/10.1001/jamanetworkopen.2024.36066

Phi, N. T. T., Oikonomidi, T., Ravaud, P., & Tran, V.-T. (2023). Assessment of US Food and Drug Administration–Approved Digital Medical Devices for Just-in-Time Interventions. JAMA Internal Medicine, 183(8), 858. https://doi.org/10.1001/jamainternmed.2023.2864

Holmes, D. R., Geoffrion, R., Hunt, J., Hance, R. ”Chip”, Leon, M. B., Mack, M. J., & Kaplan, A. V. (2022). Regulatory strategies for early device development and approval. Catheterization and Cardiovascular Interventions, 99(6), 1784–1788. Portico. https://doi.org/10.1002/ccd.30151