Publisher : FDA

FDA 21 CFR PART 58 PDF

GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES

Document status: [ Revised ]

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FDA 21 CFR PART 800 PDF

GENERAL

Document status: [ Revised ]

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FDA 21 CFR PART 803 PDF

MEDICAL DEVICE REPORTING

Document status: [ Revised ]

$36.00
FDA 21 CFR PART 803 PDF

MEDICAL DEVICE REPORTING

Document status: [ Revised ]

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FDA 21 CFR PART 806 PDF

MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS

Document status: [ Revised ]

$31.00
FDA 21 CFR PART 807 PDF

ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES

Document status: [ Revised ]

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FDA 21 CFR PART 807 PDF

ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES

Document status: [ Revised ]

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FDA 21 CFR PART 812 PDF

INVESTIGATIONAL DEVICE EXEMPTIONS

Document status: [ Active ]

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FDA 21 CFR PART 820 PDF

QUALITY SYSTEM REGULATION

Document status: [ Revised ]

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FDA 21 CFR PART 820 PDF

QUALITY SYSTEM REGULATION

Document status: [ Revised ]

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