PART 610—GENERAL BIOLOGICAL PRODUCTS STANDARDS
- SUBPART A—Release Requirements (§610.1 to §610.2)
- SUBPART B—General Provisions (§610.9 to §610.18)
- SUBPART C—Standard Preparations and Limits of Potency (§610.20 to §610.21)
- SUBPART D—Mycoplasma (§610.30 to §610.30)
- SUBPART E—Testing Requirements for Communicable Disease Agents (§610.40 to §610.48)
- SUBPART F—Dating Period Limitations (§610.50 to §610.53)
- SUBPART G—Labeling Standards (§610.60 to §610.68)