September 9, 2024- On Sept. 11 from 1-2 p.m. ET, the FDA will host a virtual Medical Device Sterilization Town Hall: Sterility Master Files and Effective Use in Premarket Submissions. The FDA is committed to reducing reliance on EtO sterilization use while ensuring the integrity of the supply chain so that patients and providers have continued access to the sterile devices they need. To meet this goal, FDA continues to take a multipronged approach, including regulatory flexibilities, supply chain analysis and mitigation, collaboration, innovation, and communication, including this regular series of town halls. Registration is not required to attend.