Regulatory Affairs Specialist II
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 Material 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.
