Michael Stadler

Michael Stadler is a Regulatory Operations Document Specialist at Sarepta Therapeutics since December 2021. Prior to this role, Michael served as a Regulatory Documentation Specialist on a contract basis through Ascent from June 2021 to November 2021, focusing on submissions archiving and process improvement. Michael's earlier experience includes working as a Regulatory Affairs Coordinator at Quark Pharmaceuticals from November 2020 to March 2021, where responsibilities included serving as a regulatory liaison and preparing technical documents for submissions. Additionally, Michael has a background in Regulatory Affairs and Operations from June 2015 to December 2017, contributing to pharmaceutical regulatory functions.