Medical Devices Expert Witnesses in New Jersey

This expert specializes in infection control. He earned his PhD in Bioengineering from the University of Pennsylvania and pursued a fellowship focused on diagnostic imaging at the Temple University School of Medicine. For two decades, he worked for a firm manufacturing automated endoscope reprocessors, serving as the Director of R&D and the Chief of Infection Control. He currently owns a consultancy focused on healthcare quality and safety; he is also a prolific writer on these issues.

This highly qualified expert earned his BS and MS in biochemistry from Victoria University of Wellington and his PhD in microbiology from Lincoln University. After completing his education, he moved to the United States to pursue a career in medical device manufacturing. He held roles as a manager of microbiological services, pharmaceutical quality control, and market product stability at Lederle Laboratories. He then worked as a director of quality control the New York blood center, director of global quality assurance and microbiological development at Wyeth and director of pharmaceutical microbiology at Merck & Co research laboratories. Most recently, he has been a senior principal scientist at Merck & Co and is currently a microbiologist at an independent consulting firm. This expert has over 70 peer-reviewed publications in microbiological journals addressing factors of contamination in medical devices. He is also a member of the United States Microbiology and Sterility Assurance Committee.

This qualified expert earned his BS in physics from University of Washington and his MS in mathematics from University of Oregeon. He also completed a MS in applied physics from the Oregon Graduate Institute of Science and Technology and his PhD in electrical engineering at Oregon Health and Science University. He subsequently entered an NIH-funded postgraduate fellowship in dermatology at the Oregon Health & Science University. After serving for a number of years as an associate professor in bioengineering and dermatology at the University of Missouri, he now directors the department of biomedical engineering at a private university in Pennsylvania.

This highly qualified expert has over 40 years of experience in medical device regulations. He received his BS in chemical engineering from Lowell Technological Institute and earned his MS in chemical engineering from the University of Iowa. He currently has 5 patents. Over the years, his work has included antimicrobial development and application, hydrophilic coating development and implementation, and over-the-counter and personal care product development. His former positions include research engineer for Eastman Kodak and GAF Corporation, project manager and laboratory supervisor for Biosearch Medical Products and Hydromer, and corporate manager of materials for Arrow International. Currently, this expert is the president of a medical device consulting company in Pennsylvania.

This highly-qualified expert has extensive experience in the field of biomaterials and biomedical engineering. He earned an MS in mechanical engineering at the University of Palermo in Italy, an MS in biomedical engineering from Imperial College London, and his PhD in biomechanics and tissue engineering at the University of Pittsburgh. He also completed a post-doctoral fellowship in tissue engineering, biomechanics, and biomaterials at the University of Palermo. This expert is active in his field as a member of several organizations, including the Tissue Engineering & Regenerative Medicine International Society, the American Society for Mechanical Engineers, and the Society for Biomaterials. He is also highly involved in research, having authored numerous publications and spoken as an invited speaker at multiple conferences throughout his career. He also currently holds 13 patents. He has previously served as an R&D engineer in the biomedical robotics and EMC department at the University Campus Biomedico Rome, a biotechnology and bioengineering consultant for the Italian Ministry for Economic Development and Livanova, a post-doctoral researcher in tissue engineering and biomechanics at the University of Pittsburgh, and a research associate in tissue engineering at the McGowan Institute for Regenerative Medicine at the University of Pittsburgh. Currently, this expert is a research assistant professor of surgery and bioengineering at a distinguished university in Pennsylvania, as well as a biotechnology and bioengineering consultant for a university-affiliated startup.

This expert has over 40 years of experience as a mechanical engineer. In addition to contributing to over 200 presentations in 38 countries, he has been extensively published in his field and is an established expert in forensic mechanical engineering. His expertise includes accident investigation and medical device liability. He now serves as a Senior Forensic Consultant for a biomechanics and biomedical engineering consulting firm.

This qualified expert has been involved in the field of medical technologies for over forty years and is experienced with matters concerning FDA compliance on which he has authored several articles and papers and given talks on FDA compliance worldwide. He is also the vice president of a private medical technologies firm, making him intimately qualified to comment on the case at hand.