Chiaki Oshima

Chiaki Oshima, with over eight years of experience in MedTech regulatory affairs in Japan, serves as a specialist at Vorpal, strategizing regulatory pathways, preparing documentation for marketing approvals, and evaluating device potential in the Japanese market. Prior to Vorpal, she worked on projects involving Class III and IV devices in respiratory, neurosurgical, and general surgical areas, collaborating with companies from over 10 countries and serving as the regulatory lead and translator, and interpreter, when needed.