Biomedical Engineering Expert Witnesses in New York

New York, New York

Biomedical Engineering, Medical Devices - Diagnostics, Instrumentation, Clinical, Biochemistry, Biomaterials, Molecular biology, Materials science, Chemistry, Medicine, Cell biology, Neurology, Organic chemistry, Device fabrication, Biosensors, Nanotechnology, Surface Plasmon Resonance, Physiology, Anatomy, Genetics, Biotechnology

I am a Biomedical Engineering PhD with multidisciplinary training in Chemistry and Medicine. I received a Bachelors in Neuroscience and Chemistry from Johns Hopkins in 2018 and then a Masters in Materials Chemistry in 2019. My research and expertise from Johns Hopkins included Nanotechnology, Materials Science, Neuroscience, Biochemistry and Biology. I then started an MD-PhD program at SUNY Downstate. I have completed the Biomedical Engineering PhD and two of the four years of medical school. My Biomedical Engineering PhD and medical coursework has given me expertise in Anatomy and Physiology (I am an Adjunct Professor at CUNY for this course), Biotechnology, Medical Devices, Biosensors, Instrumentation, Device Fabrication, and Biomaterials. I have performed research in a variety of biomedical and chemical fields and have a strong proficiency in Biosensors, Nanotechnology, Medical Devices, Diagnostics and Biomaterials. I have multiple scientific papers published and more in preparat...

New York City , New York

Medical Devices, Pharmaceutical Regulation - Medical Device FDA Regulation, Biologics FDA Regulation, FDA Compliance, FDA Warning & Labels, Product Liability, FDA Regulations, Medical Device Product Liability, Clinical Trials FDA Regulation, Medical Device FDA Approvals-Clearance, Medical Device Recalls, Medical Device Complaints, Biomedical Engineering

Dr. Ediuska Laurens is a highly credentialed biomedical engineer and expert in FDA regulation, compliance, and product liability for medical devices and biologics. She provides expert witness services to both plaintiff and defense counsel in litigation involving medical device and biologics FDA approval and clearance, labeling and warnings, quality systems, adverse event reporting, clinical trials, and post-market surveillance. Dr. Laurens brings over 20 years of combined industry, research, and regulatory experience. She has led regulatory and quality efforts across the entire medical device lifecycle, from concept through commercialization, supporting product development, regulatory submissions, and quality compliance for a wide range of technologies, including cranial and orthopedic implants, spinal and neural devices, tissue engineered-biologics and combination products, hydrogel biomaterials, as well as pediatric and women’s health innovations, among others. Attorneys rely on...