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11. Emergency use authorization of medical products and related authorities: guidance for industry and other stakeholders

12. Use of real-world evidence to support regulatory decision-making for medical devices: guidance for industry and Food and Drug Administration staff

13. Establishing the performance characteristics of in vitro diagnostic devices for the detection or detection and differentiation of human papillomaviruses: guidance for Industry and Food and Drug Administration staff

14. Data Snapshot: dislodged tubes and lines

17. CT contrast media power injectors can rupture conventional IV sets

19. Tubing misconnections: making the connection to patient safety