Publisher : FDA

FDA 21 CFR PART 58 PDF

GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES

Document status: [ Revised ]

10.20 €
FDA 21 CFR PART 800 PDF

GENERAL

Document status: [ Revised ]

9.90 €
FDA 21 CFR PART 803 PDF

MEDICAL DEVICE REPORTING

Document status: [ Revised ]

10.80 €
FDA 21 CFR PART 803 PDF

MEDICAL DEVICE REPORTING

Document status: [ Revised ]

10.80 €
FDA 21 CFR PART 806 PDF

MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS

Document status: [ Revised ]

9.30 €
FDA 21 CFR PART 807 PDF

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

Document status: [ Revised ]

10.80 €
FDA 21 CFR PART 807 PDF

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

Document status: [ Revised ]

10.80 €
FDA 21 CFR PART 812 PDF

INVESTIGATIONAL DEVICE EXEMPTIONS

Document status: [ Active ]

11.10 €
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 €