Biomedical Engineering Expert Witnesses in Illinois

Accident Reconstruction, Biomedical Engineering - accidents, biomechanics, diabetes, dynamics, energy, engineering, failure, forensics, imaging, injury, materials, mechanics, nanotechnology, neurology, neuropathy, patents, personal injury, physics, proteins, slip trip & fall, soft tissue, solar, spine, statics, statistics, vehicle

American Concrete Institute Member ASME member IEEE-EMBS Editor Author - Molecular and Cellular Biomechanics Associate Teaching Professor - Drexel University Associate Professor - University of Montana Elite Athlete - United States Rowing Team 1995 & 1997 Fire Protection Engineer - US Department of Energy - Savannah River Site Founding Member - Insurance Engineering Blockchain Consortium International Code Council Member Inventor - AFM Nanomanipulation & Surgical Patents Lunar Scientist - US Department of Energy - Office of Space Machinist - Merlin Metalworks - titanium bicycle design & Stillwater - Kevlar boat design Oath of the Engineer - Engineer's equivalent of Hippocratic Oath National Society of Professional Engineers Post-doctoral Fellow - University of Michigan MRI laboratory Recipient - Montana Governor's Innovator Award Scientist - 100+ papers and abstracts

Medical Devices, Biomedical Engineering - FDA, Medical Devices, FDA Compliance, FDA law, FDA Inspections, FDA medical device regulation, FDA medical device labeling, FDA regulation of clinical trials, FDA approval of medical devices. Medical Device Recalls, Medical Device Complaints, FDA Inspections

A recognized expert on the FDA regulation of Medical Devices. Experience as an expert witness involving medical device firms and FDA requirements regarding approvals, recalls, complaint investigations, and labeling. Over 20 years of FDA experience encompassing virtually all of the FDA field positions. Also eighteen years of industry experience as a mid-level manager and senior executive in clinical, regulatory, and quality in the medical device industry. Personally designed quality systems, prepared regulatory submissions (510(k), IDE and PMA) and managed 7 multi-center clinical trials for class 3 medical devices. From 1989-1993, was the Industry Representative on the FDA Circulatory Systems panel which reviewed over 30 PMA clinical studies for cardiovascular device. Serve as an expert witness for cases involving FDA regulation compliance for medical devices. Regularly perform webinars regarding FDA and issues regarding clinical studies and medical devices. Finally, a ...