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DPDP Act compliance check for companies
, core duties apply from 13 May 2027
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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 111 — CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Subpart P — Records and Recordkeeping
Federal (United States) · Regulations
Subpart P — Records and Recordkeeping
2 sections
2 sections
21 C.F.R. § 111.605
What requirements apply to the records that you make and keep?
21 C.F.R. § 111.610
What records must be made available to FDA?
Subpart P — Records and Recordkeeping | Federal (United States) Regulations | Justis AI