Paper Details

Paper Title

Assessing the cost burden of United States FDA-mandated post-approval studies for medical devices.

Paper Journal Title

J Health Care Finance

Paper Citation Count

Paper Publication Year

2016

Bio Mention

PAS

Mesh Descriptor

Costs and Cost Analysis, Device Approval, Equipment Design, Humans, Safety, United States, United States Food and Drug Administration

Author Name	Affiliation
Neil J Wimmer
Susan Robbins	Comparative Effectiveness Research Institute and Department of Cardiovascular Medicine, Lahey Clinic Foundation
Henry Ssemaganda	Comparative Effectiveness Research Institute and Department of Cardiovascular Medicine, Lahey Clinic Foundation
Erin Yang	Comparative Effectiveness Research Institute and Department of Cardiovascular Medicine, Lahey Clinic Foundation
Sharon-Lise T Normand	Harvard Medical School, Harvard T.H. Chan School of Public Health
Michael Matheny	Geriatrics Research Education and Clinical Center (GRECC), Tennessee Valley Healthcare System, TN Vanderbilt University School of Medicine
Michael E Matheny	Geriatrics Research Education and Clinical Center (GRECC), Tennessee Valley Healthcare System, TN Vanderbilt University School of Medicine
Naomi Herz
Josh Rising
Frederic S Resnic	Comparative Effectiveness Research Institute and Department of Cardiovascular Medicine, Lahey Clinic Foundation, USA Tufts University School of Medicine

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