FDA Reissues Cybersecurity Guidance: Strategic Alignment with QMSR and ISO 13485

Review of Drug Master Files in Advance of Certain ANDA Submissions Under GDUFA

The U.S. Food and Drug Administration’s (FDA) reissued final guidance regarding quality system management considerations for medical device cybersecurity. The update marks the official transition from the old Quality System Regulation (QSR) to the new Quality Management System Regulation (QMSR), directly integrating ISO 13485:2016 standards.