||Development document for interim final effluent limitations guidelines and proposed new source performance standards for the pharmaceutical manufacturing point source category.
||Environmental Protection Agency, Washington, DC. Effluent Guidelines Div.
|| U.S. Environmental Protection Agency, Office of Water and Hazardous Materials, Effluent Guidelines Division ; Available from the National Technical Information Service,
Pharmaceutical chemistry--Waste disposal. ;
Pharmaceutical research--United States.
Drug industry ;
Water pollution control ;
Chemical effluents ;
Pollution regulations ;
Industrial waste treatment ;
Industrial water ;
Waste water treatment ;
Point sources ;
Industrial plants ;
Water pollution sampling ;
Water pollution standards ;
Environmental impacts ;
Water pollution economics ;
Economic impact ;
Pharmaceutical manufacturing ;
Treatment technology ;
New Source Performance Standards ;
BAT(Best available technology)
||Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy.
||358 pages : illustrations, maps ; 28 cm
This document presents the findings of a study of the pharmaceutical manufacturing point source category for the purpose of developing effluent limitations and guidelines for existing point sources plus standards of performance and pretreatment standards for existing and new sources. Effluent limitations were developed on the basis of the level of raw waste load and the degree of treatment achievable by suggested model systems.
"EPA 440/1-75/060, Group II"--Cover. "December 1976." Includes bibliographical references (281-295). Microfiche.