Title 21--Food and Drugs

CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

PART 820--QUALITY SYSTEM REGULATION


TEXT PDF820.1 Scope.
TEXT PDF820.3 Definitions.
TEXT PDF820.5 Quality system.
TEXT PDF820.20 Management responsibility.
TEXT PDF820.22 Quality audit.
TEXT PDF820.25 Personnel.
TEXT PDF820.30 Design controls.
TEXT PDF820.40 Document controls.
TEXT PDF820.50 Purchasing controls.
TEXT PDF820.60 Identification.
TEXT PDF820.65 Traceability.
TEXT PDF820.70 Production and process controls.
TEXT PDF820.72 Inspection, measuring, and test equipment.
TEXT PDF820.75 Process validation.
TEXT PDF820.80 Receiving, in-process, and finished device acceptance.
TEXT PDF820.86 Acceptance status.
TEXT PDF820.90 Nonconforming product.
TEXT PDF820.100 Corrective and preventive action.
TEXT PDF820.120 Device labeling.
TEXT PDF820.130 Device packaging.
TEXT PDF820.140 Handling.
TEXT PDF820.150 Storage.
TEXT PDF820.160 Distribution.
TEXT PDF820.170 Installation.
TEXT PDF820.180 General requirements.
TEXT PDF820.181 Device master record.
TEXT PDF820.184 Device history record.
TEXT PDF820.186 Quality system record.
TEXT PDF820.198 Complaint files.
TEXT PDF820.200 Servicing.
TEXT PDF820.250 Statistical techniques.

















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