Dr Eric Qin is the VP of Regulatory and Clinical Affairs at SeeTreat. He has over 10 years of experience in medical device quality and global regulations across both the private and public sectors, including senior leadership roles at the Therapeutic Goods Administration (TGA) as an assistant director and QMS auditor.
His expertise extends across the design and development of Sterile devices, Implantables, Software as a Medical Device (SaMD), In Vitro Diagnostics Devices (IVD), and AI as a Medical Devices (AIaMD). He is particularly interested in the application of Artificial Intelligence (AI) and Deep Learning technologies in healthcare, with a focus on exploring how these technologies can support clinicians in achieving enhanced patient outcomes.