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US law
Federal (United States)
Regulations
Title 40 CFR — Protection of Environment
Chapter I — ENVIRONMENTAL PROTECTION AGENCY
Part 439 — PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
Federal (United States) · Regulations
Part 439 — PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
41 sections
5 groups
Subpart A — Fermentation Products
8 sections
Subpart B — Extraction Products
8 sections
Subpart C — Chemical Synthesis Products
8 sections
Subpart D — Mixing/Compounding and Formulation
8 sections
Subpart E — Research
3 sections
6 sections filed directly here
40 C.F.R. § 439.0
Applicability.
40 C.F.R. § 439.1
General definitions.
40 C.F.R. § 439.2
General monitoring requirements.
40 C.F.R. § 439.3
General pretreatment standards.
40 C.F.R. § 439.4
General limitation or standard for pH.
40 C.F.R. Appendix A to Part 439
Tables
Part 439 — PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY | Federal (United States) Regulations | Justis AI