PART 439—PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
- 439.0—Applicability.
- 439.1—General definitions.
- 439.2—General monitoring requirements.
- 439.3—General pretreatment standards.
- 439.4—General limitation or standard for pH.
- SUBPART A—Fermentation Products (§439.10 to §439.17)
- SUBPART B—Extraction Products (§439.20 to §439.27)
- SUBPART C—Chemical Synthesis Products (§439.30 to §439.37)
- SUBPART D—Mixing/Compounding and Formulation (§439.40 to §439.47)
- SUBPART E—Research (§439.50 to §439.52)