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Records and Reports

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Biologics
  6. Current Good Manufacturing Practice for Blood and Blood Components
  7. Records and Reports

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Section
606.160

Records.

Section
606.165

Distribution and receipt; procedures and records.

Section
606.170

Adverse reaction file.

Section
606.171

Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services.

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