RAPID - Key Publications

Malone, M. (2018). SPEED: A New Initiative in Real-World PAD Evidence Evaluation. An overview of the FDA’s new multistakeholder project to support real-world evidence evaluation for devices aimed at treating peripheral artery disease. Endovascular Today 17.9 (2018): 57-60.

 

Registry Assessment of Peripheral Interventional Devices (RAPID) Phase II Global Unique Device Identification (GUDID)/Informatics Work Group Summary

 

Shuren, J., & Califf, R. M. (2016). Need for a National Evaluation System for Health Technology. Jama. doi:10.1001/jama.2016.8708

 

Morales, J.P.,  Cronenwett, J, Thatcher, R. (2016). Registry Assessment of Peripheral Interventional Devices (RAPID). Endovascular Today 15.8 (2016): 85-94.

 

Jones W.S., Krucoff M.W., Morales P., Wilgus R.W., Heath A.H., Williams M.F., Tcheng J.E., Marinac-Dabic J.D., Malone M.L., Reed T.L., Fukaya R., Lookstein R.A., Handa N., Aronow H.D., Bertges D.J., Jaff M.R., Tsai T.T., Smale J.A., Zaugg M.J., Thatcher R.J., Cronenwett J.L. Registry Assessment of Peripheral Interventional Devices (RAPID): Registry assessment of peripheral interventional devices core data elements. (2018). NCBI PMID:29389426

 

W. Jones-Mitchell Krucoff-Pablo Morales Registry Assessment of Peripheral Interventional Devices (RAPID)― Registry Assessment of Peripheral Interventional Devices Core Data Elements. (2018). Journal of Vascular Surgery,82(2), 316-322.

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