Biomedical Engineering Expert Witnesses in Illinois

The SEAK Expert Witness Directory contains a comprehensive list of biomedical engineering expert witnesses who testify, consult and provide litigation support on biomedical engineering and related issues. Biomedical engineering expert witnesses and consultants on this page may form expert opinions, draft expert witness reports, and provide expert witness testimony at deposition and trial. The issues and subjects these biomedical engineering expert witnesses testify regarding may include: Fda Inspections, Airway Management, Ambulatory Anesthesia, Drug Errors, Epidural And Spinal Anesthesia, Failed Intubation, FDA, Fda Approval Of Medical Devices, Fda Compliance, Fda Law, Fda Medical Device Labeling, Fda Medical Device Regulation, Fda Regulation Of Clinical Trials, General Anesthesia, and Intraoperative And Postoperative Complications.

Use the search box above to further refine your search for biomedical engineering expert witnesses by keyword and state. Attorneys contact the experts directly – with no middleman.

Bradley E Layton, PhD PE Human Powered Future PLLC

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

Sasha M Demos, MD, PhD Dupage Valley Anesthesiologists

Naperville, Illinois
Anesthesiology, Biomedical Engineering - Airway Management, Failed Intubation, Epidural and Spinal Anesthesia, Obstetrical Anesthesia, General Anesthesia, Surgical Fires, Drug Errors, Positioning Injuries, Regional Anesthesia, Ambulatory Anesthesia, Intraoperative and Postoperative Complications, Sedation Complications Outside of the OR
Board certified anesthesiologist and Chairman of the Department of Anesthesia at a large community hospital. PhD in Bioengineering with research and publications in the areas of liposomes, ultrasound contrast agents, and targeted therapies. Administrative experience has provided involvement in the areas of quality, drug diversion prevention and risk management. Extensive experience in airway management, prevention of surgical fires, general, obstetrical, pediatric, thoracic, neuro, regional, and ambulatory anesthesia as well as sedation outside of the operating room.

J. Lawrence Stevens, RAC ONE WAY CONSULTANTS. LLC, FDA Regulatory Experts

East Alton, Illinois
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 ...
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