Search Results for the EPA National Library Catalog

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Select Item Title Year Published
American pharmaceutical review. 1998
Analytical methods for the determinatiion of pollutants in pharmaceutical manufacturing industry wastewater. 1998
Analytical methods for the determination of pollutants in pharmaceutical manufacturing industry wastewater. 1995
Biopharmaceuticals in transition 1990
Chemical industry 1994
Compliance Assistance Tool for CCA Regulations: Subpart GGG of 40 CFR Part 63 - NESHAPs for Source Category Pharmaceuticals Production. 2002
Compliance assistance tool for Clean Air Act regulations : subpart GGG of 40 CFR Part 63 NESHAPS for source category pharmaceutical production. 2002
Compliance assistance tool for pharmaceutical production, pesticide active ingredient production, and miscellaneous organic chemical manufacturing NESHAP : comparison of regulatory requirements and case study compliance illustrations for nondedicated equipment / 2004
Contractor's engineering report for the development of effluent limitations guidelines and standards for the pharmaceutical manufacturing industry point source category / 1980
Cost effectiveness analysis of effluent limitations and standards for the pharmaceutical industry / 1982
Cost effectiveness analysis of effluent standards and limitations for battery manufacturing / 1984
Cost-effectiveness analysis of final effluent limitations guidelines and standards for the pharmaceutical manufacturing industry. 1998
Development document for effluent guidelines, new source performance standards and pretreatment standards for the pharmaceutical manufacturing point source category / 1982
Development document for effluent limitations quidelines and standards for the pharmaceutical manufacturing point source category / 1983
Development document for final best conventional technology effluent limitations guidelines for the pharmaceutical manufacturing point source catagory. 1986
Development document for final effluent limitations guidelines and standards for the pharmaceutical manufacturing point source category. 1998
Documentation basics : that support good manufacturing practices and quality system regulations / 2001
Drug repositioning : bringing new life to shelved assets and existing drugs / 2012
Drug truths : dispelling the myths about pharma R & D / 2009
Dun & Bradstreet/Gale Group industry handbook : chemicals and pharmaceuticals / 2000
Economic analysis of effluent standards and limitations for the pharmaceutical industry / 1983
Economic analysis of final effluent limitations guidelines and standards for the pharmaceutical manufacturing industry. 1998
Economic analysis of proposed effluent standards and limitations for the pharmaceutical industry / 1982
Economic impact and regulatory flexibility analysis of proposed effluent guidelines for the pharmaceutical manufacturing industry : final report. 1995
Enhanced COD (Chemical Oxygen Demand) Removal from Pharmaceutical Wastewater Using Powdered Activated Carbon Addition to an Activated Sludge System. 1985
Environmental assessment of the final effluent limitations guidelines and standards for the pharmaceutical manufacturing industry. 1998
Environmental assessment of the proposed effluent guidelines for the pharmaceutical manufacturing industry. 1995
EPA Office of Compliance Sector Notebook Project. Profile of the pharmaceutical manufacturing industry. 1997
EPA's 33/50 program company profile : Bristol-Myers Squibb Company. 1995
Evaluation of activated carbon for enhanced COD removal from pharmaceutical wastewater / 1985
Evaluation of activated carbon for enhanced COD removal from pharmaceutical wastewater : Volume 2. Appendices / 1985
Glocal pharma international brands and the imagination of local masculinity / [electronic resource] : 2016
Guides to pollution prevention : the pharmaceutical industry. 1991
Guides to pollution prevention : the pharmaceutical industry. 1991
Laboratory validation 2003
National emission standards for hazardous air pollutants (NESHAP) for the pharmaceutical manufacturing industry : background information for promulgated standards, summary of public comments and responses / 1998
OPD chemical buyers directory. 1969
Permit guidance document : pharmaceutical manufacturing point source category (40 CFR Part 439) / 2006
Pharmaceutical industry : hazardous waste generation, treatment, and disposal. 1976
Pharmaceuticals manufacture 1991
Pollution prevention assessment for a manufacturer of pharmaceuticals / 1995
Preliminary data summary for the pharmaceutical manufacturing point source category. 1989
Product development planning for health care products regulated by the FDA 1997
Profile of the pharmaceutical manufacturing industry. 1997
Re-inventing drug development / 2015
Regulatory impact assessment of proposed effluent guidelines for the pharmaceutical manufacturing industry : final report. 1995
Statistical support document for final effluent limitations guidelines and standards for the pharmaceutical manufacturing industry. 1998
Volatile organic compound emission controls for tablet coating at pharmaceutical plants / 1984
Waste audit study, drug manufacturing and processing industry 1989
Waste treatment and disposal methods for the pharmaceutical industry / 1975
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