Content of Human Factors Information in Medical Device Marketing Submissions: Draft Guidance for Industry and Food and Drug Administration Staff
Detailed guidance document from FDA and regulatory agencies.
Document Details
Guidance Document
December 9, 2022
December 8, 2022
6b81845f-385d-4062-90f7-c9f35edefab7
Related Documents
Computer Software Assurance for Production and Quality Management System Software: Guidance for Industry and Food and Drug Administration Staff
Guidance DocumentFebruary 3, 2026Center for Devices and Radiological Health
Dental Curing Lights - Premarket Notification (510(k)) Submissions: Draft Guidance for Industry and Food and Drug Administration Staff
Guidance DocumentJuly 12, 2024Center for Devices and Radiological Health
Computer Software Assurance for Production and Quality System Software: Draft Guidance for Industry and Food and Drug Administration Staff
Guidance DocumentSeptember 13, 2022Center for Devices and Radiological Health
Quick Actions
Transform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.
Try KeyPedia Today
Explore our real use cases and discover our features in depth.
Subscribe to our newsletter
Get the latest updates and insights delivered to your inbox