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Permit Guidance Document: Pharmaceutical Manufacturing Point Source Category (PDF)(88 pp, 757 K,
January 2006,
821-F-05-006)
Assists permit writers and pretreatment coordinators in developing appropriate NPDES permits and pretreatment requirements for pharmaceutical facilities
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Development Document for Final Effluent Limitations Guidelines and Standards for the Pharmaceutical Manufacturing Point Source Category (PDF)(468 pp, 1 MB,
July 1998,
821-R-98-005)
Describes industry processes, pollutants generated, available control and treatment technologies, the technical basis for the final rule, and costs of the rule
- Economic Analysis of Final Effluent Limitations Guidelines and Standards for the Pharmaceutical Manufacturing Industry (PDF)(295 pp, 933 K, July 1998, 821-B-98-009)
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Analytical Methods for the Determination of Pollutants in Pharmaceutical Manufacturing Industry Wastewater (PDF)(99 pp, 217 K,
July 1998,
EPA 821-B-98-016)
Compendium of Methods 1666, 1667 and 1671; to support Pharmaceutical Manufacturing Effluent Guidelines
- Analytical Method Guidance for the Pharmaceutical Manufacturing Point Source Category (PDF)(34 pp, 124 K, August 1999, 821-B-99-003)
- Pharmaceutical Manufacturing Effluent Guidelines - Final Rule (PDF)(24 pp, 3 MB, October 27, 1983, 48 FR 49808)
- Pharmaceutical Manufacturing Effluent Guidelines - Interim Final Rule (PDF)(11 pp, 2 MB, November 17, 1976, 41 FR 50676)
US EPA
United States Environmental Protection Agency