Part 320. PART 320—BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS

• SUBPART A [§ 320.1 - § 320.1] - Subpart A—General Provisions
• SUBPART B [§ 320.21 - § 320.63] - Subpart B—Procedures for Determining the Bioavailability or Bioequivalence of Drug Products