Publisher : FDA

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FDA 21 CFR PART 820 PDF

QUALITY SYSTEM REGULATION

Document status: [ Revised ]

10.20 €
FDA 21 CFR PART 820 PDF

QUALITY SYSTEM REGULATION

Document status: [ Revised ]

10.20 €
FDA 21 CFR PART 820 PDF

QUALITY SYSTEM REGULATION

Document status: [ Revised ]

10.20 €
FDA 21 CFR PART 821 PDF

MEDICAL DEVICE TRACKING REQUIREMENTS

Document status: [ Revised ]

9.30 €
FDA 21 CFR PART 830 PDF

UNIQUE DEVICE IDENTIFICATION

Document status: [ Revised ]

9.60 €
FDA 21 CFR PART 830 PDF

UNIQUE DEVICE IDENTIFICATION

Document status: [ Revised ]

9.60 €
FDA 21 CFR PART 898 PDF

PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES

Document status: [ Revised ]

8.40 €
FDA 21 CFR UCM 094461 PDF

Medical Device Use-Safety: Incorporating Human Factors Engineering into Risk Management

Document status: [ Active ]

12.90 €
FDA 21 CFR UCM 259748 PDF

Applying Human Factors and Usability Engineering to Medical Devices

Document status: [ Active ]

14.70 €
FDA Regulatory Affairs PDF

Document status: [ Active ]

79.20 €
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