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Titles
- Unique Device Identification System: form and content of the unique device identifier (UDI) : guidance for industry and Food and Drug Administration staff1
- Unique device identification: Policy regarding compliance dates for class I and unclassified devices, direct marking, and Global Unique Device Identification Database requirements for certain devices : guidance for industry and Food and Drug Administration staff1
- Use of real-world evidence to support regulatory decision-making for medical devices: guidance for industry and Food and Drug Administration staff1