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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Part 606 — CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
Subpart I — Records and Reports
Federal (United States) · Regulations
Subpart I — Records and Reports
4 sections
4 sections
21 C.F.R. § 606.160
Records.
21 C.F.R. § 606.165
Distribution and receipt; procedures and records.
21 C.F.R. § 606.170
Adverse reaction file.
21 C.F.R. § 606.171
Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services.
Subpart I — Records and Reports | Federal (United States) Regulations | Justis AI