Regulatory Affairs Specialist

Brandie Moore

Brandie is a Regulatory Affairs Specialist II for MedVenture Health. As part of the regulatory team, Brandie responsibilities include preparation of regulatory submissions, document reviews, internal audits, and handles Reach, RoHS, Prop-65 compliance requests.

Since joining MedVenture in 2016, Brandie has contributed to various regulatory projects, including successfully clearing multiple 510(k)’s and a CE Mark. With the knowledge and experience that Brandie has gained, she was able to complete of the Regulatory Affairs Certificate for Medical Devices in 2018.