
Key Concepts for Medical Device Testing
Recorded: July 2023
This webinar discusses why in vivo testing is needed for regulatory approval of a Medical Device and what specific testing is required.
Agenda
- Introduction
- Development of innovative Medical Devices
- Challenges of in vivo testing
- How to succeed in the in vivo testing phase
- Capabilities and expertise
Moderated by:
Mehdi Doroudchi, Ph.D. – Sr. Director of CGT & Scientific Affairs at Pharmaron
Speaker
Marina Mamarian, DVM – Senior Veterinary Scientist at Pharmaron
Dr. Mamarian is a veterinarian specializing in large animal medicine, having received her DVM from the University of Buenos Aires and a translational science certification from UC San Diego. After serving as the scientific communication lead for Latin America at Royal Canin and a research associate at Yale University School of Medicine, Dr. Mamarian is now a Senior Veterinarian Scientist and Study Director for Medical Device Coordination and execution of in vivo studies at Pharmaron’s facility in San Diego. She has worked with over 30 research groups and 15 leader companies in the biomedical field, leading, overseeing and executing over 500 successful studies involving surgical procedures on large animal models. She is also the co-author on 7 papers and is motivated by the belief that “Translational Research Saves Lives” and in the power of interdisciplinary teams working toward one major goal: innovating medicine to improve the health of patients worldwide.