Code of Federal Regulations · Part

Part 439 — Pharmaceutical Manufacturing Point Source Category

40 C.F.R. pt. 439

• § 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
• Subpart B Extraction Products
• Subpart C Chemical Synthesis Products
• Subpart D Mixing/compounding And Formulation
• Subpart E Research