Part 439. PART 439—PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY

• SUBPART A [§ 439.10 - § 439.17] - Subpart A—Fermentation Products
• SUBPART B [§ 439.20 - § 439.27] - Subpart B—Extraction Products
• SUBPART C [§ 439.30 - § 439.37] - Subpart C—Chemical Synthesis Products
• SUBPART D [§ 439.40 - § 439.47] - Subpart D—Mixing/Compounding and Formulation
• SUBPART E [§ 439.50 - § 439.52] - Subpart E—Research
• SUBPART 0 -

• General

  • SECTION § 439.0 - Applicability.
  • SECTION § 439.1 - General definitions.
  • SECTION § 439.2 - General monitoring requirements.
  • SECTION § 439.3 - General pretreatment standards.
  • SECTION § 439.4 - General limitation or standard for pH.

• APPENDIX

  • Appendix A to Part 439—Tables