EXPERT NUMBER: 3660. STATE: FL. REGION: Eastern, Southeast, Southern. COUNTRY: United States Expert Witnesses.
Provides Opinion & Testimony In:
Cardiac Device, Cardiac Pacemakers, Implantable Cardiac Defibrillator, Cardiac Imaging, Cardiac Stents, Atrial Fibrillation, Cardiovascular Devices, Medical Device R&D Engineer, Biomedical Engineering, Cardiovascular Signal Analysis, Medical Device Design, Interventional Cardiovascular Devices, Cardiac Pacing Devices, Cardiac Stents, Artificial Organ Design, Neuro Modulation, Biocompatibility Studies, FDA Device Controls & Regulatory Issues, CNS Epilepsy, Neurology, Cardiology, Cardiac Echo Imaging, Nuclear Medicine, MRI, CT Imaging, Cardiac Echocardiography, Patent Prosecution, Echocardiography, Bio Synch Nautilus Medical Device Heart Rate Monitor, Design Electronic Circuit, Systems Control, Cardiac Resynchronization Management Therapy Devices, Artificial Organ Design, Cardiac Echocardiography, Medical Device Project Management, Neurological Therapy Devices, Cardiac Electrophysiology, FDA Device Design Controls, Patent Prosecution, Cardiac Implantable Devices, Implantable Cardiac Pacing, Implantable Cardiac Defibrillator Devices,Cardiac Resynchronization Devices Including Both Pacemaker ICD Devices From Medtronic & Boston Scientific Corporation, Device Failure Cases Implantable Cardiac Defibrillators Medical Devices,Full Body Imaging Technology, Ventilator, Respitory Monitoring Equipment, Depuy,
EXPERT NUMBER: 1779. STATE: MN. REGION: Central, Eastern, Midwest, Western. COUNTRY: United States Expert Witnesses.
Provides Opinion & Testimony In:
Medical Device, Pharmaceutical, FDA, Medical Products Liability, Defective Medical Devices, Medical Device Labeling, Medical Device Manufacturing, Quality Assurance, Clinical Evaluation, Clinical Studies, Medical Device Human Factors, Medical Device Personal Injury/Death
EXPERT NUMBER: 1957. STATE: OH. REGION: Eastern, Midwest, Northeast. COUNTRY: United States Expert Witnesses.
Provides Opinion & Testimony In:
Quality Management, FDA Compliance certification of medical device manufacturing, Quality systems development, Gap Analysis, Standards Compliance, ISO QS Desk Quality Audits, Process control, Quality Manual, FDA 820 compliance, ISO 9000, ISO 2000 ISO 13485 registration, Quality System development and management, ISO Systems and / internal auditing, Technical files (TF) development, submission and support, ISO 13485, ISO 9001, ISO 14971, and ISO 17025 support, Quality System Regulations support, FDA 483 Warning letter and remediation support, ISO registration support, Supplier management of domestic/ overseas manufacturers, Complaint handling management, Document control management, Inspection systems and controls, Calibration systems, 510(k) development, submission, and support
Medical Device manufacturing support
EXPERT NUMBER: 3008. STATE: CA. REGION: Pacific, Southwestern, Western. COUNTRY: United States Expert Witnesses.
Provides Opinion & Testimony In:
Medical Products, Devices, Safety, Efficacy, Intellectual Property Analysis, Patent Infringement, Clinical Studies, Least Invasive, Surgical Therapies, Product, Process Development, Surgically Implanted Mesh
EXPERT NUMBER: 986. STATE: TX. REGION: Central, Southern, Southwestern, Western. COUNTRY: United States Expert Witnesses.
Provides Opinion & Testimony In:
Biomedical Engineer, Electrical Engineer, Certified Clinical Engineer, Patent, Medical Devices, Product Liability, International Health Care Safety Professionals, Biomedical Devices, FDA Neurological Devices, Laser Device Instructions For Use, Manuals, Labels Warnings, Department of Health Human Services, FDA, Kugel Mesh Hernia Patch, Radiological Equipment, FDA Regulatory Issues, Medical Devices Life Cycle, Medical Device, Equipment, Safety, Biomedical, Clinical engineering, infusion pump, ESU, laser, Monitor, Equipment Labeling, Healthcare technology, compliance, Risk, Equipment repair, Maintenance, Medical technology life cycle, Wireless networks, FDA, Telemedicine, Regulation, Defect, patent IP.
