Terrie L. Reed

Statistics

Publications

Citations

H-Index

Active since

2010

Affiliations

United States Food and Drug Administration(Current)

Clinical Research Institute

Terrie L. Reed is an author at United States Food and Drug Administration specializing in medical device safety, device documentation, and device-related adverse event reporting.

ORCID

Publications per year

2010–2018

Publications

Registry Assessment of Peripheral Interventional Devices (RAPID): Registry assessment of peripheral interventional devices core data elements

W. Schuyler Jones, Mitchell W. Krucoff, Pablo Morales et al. · Journal of Vascular Surgery · 2018 · 19 citations · Full text

Law, Biomedical Informatics, Health Technology Assessment +14

FDA Adverse Event Problem Codes: Standardizing the Classification of Device and Patient Problems Associated with Medical Device Use

Terrie L. Reed, Diana Kaufman-Rivi · Biomedical Instrumentation & Technology · 2010 · 18 citations

Health Professions, Health Services Administration, Clinical Classification Systems +16

Advancing medical device innovation through collaboration and coordination of structured data capture pilots: Report from the Medical Device Epidemiology Network (MDEpiNet) Specific, Measurable, Achievable, Results-Oriented, Time Bound (SMART) Think Tank

Terrie L. Reed, Joseph P. Drozda, Kevin M. Baskin et al. · Healthcare · 2016 · 15 citations

Engineering, Biomedical Engineering, Health Informatics +17

1–3 of 3