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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 320 — BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
Federal (United States) · Regulations
Part 320 — BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
19 sections
2 groups
Subpart A — General Provisions
1 section
Subpart B — Procedures for Determining the Bioavailability or Bioequivalence of Drug Products
18 sections
Part 320 — BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS | Federal (United States) Regulations | Justis AI