Where to find FDA software and cybersecurity submission requirements

Webinar : How to Meet FDA Cybersecurity Standards for Medical Devices | QualysecПодробнее

Mastering FDA eSTAR Cybersecurity Requirements for 510(k) SubmissionsПодробнее

FDA Cybersecurity Testing Requirements - Interview with Red SentryПодробнее

Webinar: Medical Devices Cybersecurity in 510(k) Premarket SubmissionsПодробнее

Webinar: The FDA ‘Cybersecurity Refuse to Accept Policy’ will affect Medical Device Manufacturers!Подробнее

FDA Cybersecurity and Software Policy Updates: Navigating the New FDA Guidance Documents for MedTechПодробнее

Navigating FDA’s New Cyber Device Paradigm - Cybersecurity & Compliance, Industry Best PracticesПодробнее

Demystifying FDA’s Pre-Market Final GuidanceПодробнее

FDA Cybersecurity Guidance FinalizedПодробнее

Using the new eSTAR templates for a 510(k) submission and the FDA eSTAR draft guidanceПодробнее

Webinar // Cybersecurity in the medical devices – How to show compliance to regulatory requirementsПодробнее

FDA Cybersecurity in Medical DevicesПодробнее

How to prepare an FDA eSTAR 510(k) submissionПодробнее

Prepare Your Medical Devices for the Latest FDA Cybersecurity GuidelinesПодробнее

Software Validation Documentation for FDA 510(k) pre-market notification submissionПодробнее

Cybersecurity Labeling RequirementsПодробнее

Are you Prepared for Upcoming FDA Cybersecurity Deadlines?Подробнее

Cybersecurity Webinar - Learn what the FDA wants in your 510(k)Подробнее

Cybersecurity Documentation for a 510(k) SubmissionПодробнее