Jason Gerhold

Jason Gerhold joined Invivoscribe in 2012 and serves as the Global Director of Regulatory, Quality, and Clinical Affairs focusing on developing high-quality diagnostics that meet both international pathology needs and support pharma partner’s drug development programs. He directly manages employees in the US, Japan, and China, and is responsible for worldwide compliance to relevant laws, regulations, and standards.

Jason Gerhold joined Invivoscribe in 2012 and serves as the Global Director of Regulatory, Quality, and Clinical Affairs focusing on developing high-quality diagnostics that meet both international pathology needs and support pharma partner’s drug development programs. He directly manages employees in the US, Japan, and China, and is responsible for worldwide compliance to relevant laws, regulations, and standards.