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GMP Expert Witnesses testifying in Litigation

GMP experts in this Medical Devices directory provide witness opinion and testimony in all types of GMP accidents including Toxicology Air emissions of volatiles, Toxicology Pharmaceutical solids, Toxicology Emergency response plan, Toxicology training and FDA Consultant Supplements.

GMP accidents can occur in GLP, GCP Compliance, Regulatory Issues, Risk Management and 510K.

In litigation, GMP accident experts attempt to use forensic engineering and biomechanical engineering research to reconstruct the accident and damages or event by providing witness testimony, computer animation or graphical exhibits to opine in a compelling way to the jury

Medical Devices Expert Witnesses for Attorneys

Search results for: GMP

Pharmaceutical Oncology Expert Witness No.3033
Provides Opinion & Testimony In:
State: MD
Region: Eastern, Northeast
Country: US
Pharmaceutical, New Drug Application Under FDA, Medical Imaging, Oncology, Pain Management, Anti Infectives, Ophthalmics, Drug Development, Drug Identification, Drug Labeling, Drug Labels, Drug Warnings, Drug Safety, FDA Medical Device Regulation, FDA New Drug Review Approval Procedures, Medical Devices, Pharmaceutical Development, Pharmaceutical Process Chemistry, Pharmaceutical Science, Pharmaceuticals, Pharmaceuticals Manufacturing, Pharmaceuticals Regulatory Affairs, Quality Assurance, GXP, GMP, GLP, GCP Compliance, Regulatory Issues, Risk Management, Review FDA Correspondence,
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State: TX
Region: Central, Southwest
Country: US
Patent Infringement, Implants, Medical Devices, Surgical Devices, Surgical Implants, FDA, Freedom Operate, 510K, PMA, Class 3 Medical Device, IDE PMA, HCTP, Products Liability, Cartilage, Orthopedics, Orthopedic Surgery, Sports Medicine, Material Science, Use Errors, Medical Device Testing, Human Factors, Engineering, Patient Safety, Biomedical Engineering, Clinical Engineering, Medical Device Service Management, Cervical Spine, Extremity Trauma, Workmens Compensation, Biological Implants, Xenotransplantation, Allografts, Autologous Grafts, Biological Devices, Xenotransplants, Osteomyeliti...
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State: PA
Region: Eastern, Northeast
Country: US
FDA Regulatory Affairs Professional, Certified FDA Regulatory Affairs, Regulatory Compliance Quality Assurance Functions, FDA Regulatory Affairs Drug Manufacturers, FDA Regulatory Affairs Equipment Facility Implementation, FDA Regulatory Affairs Quality Assurance, FDA Regulatory Affairs Drug Process Manufacturing Investigation, FDA Regulatory Affairs,
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State: NV
Region: Pacific, Southwest
Country: US
Product Design Mechanical Engineer, Engineer, Mechanical Design Product Development, Product Design Mechanical Engineer, products, development, materials, manufacturing, consumer products, medical equipment, power tools, automotive systems, failure analysis, equipment automation, control systems machine guarding, control, operator training, fabrication processes, plastic injection molding, total product development expertise, Marketing, Manufacturing, Quality Product Regulations, design validation, industry consensus standards, customized Machine guarding, Lockout Tagout, AutoCad, Design p...
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