Record Display for the EPA National Library Catalog
RECORD NUMBER: 190 OF 880Main Title | Compliance Assistance Tool for CCA Regulations: Subpart GGG of 40 CFR Part 63 - NESHAPs for Source Category Pharmaceuticals Production. | |||||||||||
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CORP Author | Environmental Protection Agency, Washington, DC. Office of Enforcement and Compliance Assurance. | |||||||||||
Year Published | 2002 | |||||||||||
Report Number | EPA-301-B-01-005 | |||||||||||
Stock Number | PB2010-110684 | |||||||||||
Additional Subjects | Air pollution control ; Pharmaceutical industry ; Compliance ; Regulations ; Clean Air Act ; Emission ; Control systems ; Air quality standards ; Monitoring ; Waste water treatment ; US EPA ; Statutes ; Performance evaluation | |||||||||||
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Collation | 258p | |||||||||||
Abstract | This document is intended to help owners and operators of pharmaceutical manufacturing operations understand and comply with U.S. Environmental Protection Agency's (EPA) air pollution regulations promulgated on September 21, 1998, substantially revised on August 29, 2000 and revised again on August 2, 2001, for the pharmaceutical industry. These regulations contain new emissions standards based on the 'maximum achieveable control technology' or MACT. On September 21, 1998, EPA published new effluent guidelines, pretreatment standards pursuant to the Clean Water Act (CWA). These new CWA provisions are not reviewed in this document. |