Air Toxics Website: Rule and Implementation Information for Pharmaceuticals Production Industry

(Docket# A-96-03

last updated

From the listing below, find the file you would like to download.

Rule Information Technical formation Implementation Information

Rule Information

Proposed and Promulgated Rules

Subpart GGG - National Emission Standards for Pharmaceuticals Production

Date	Citation)	Action	Description	File Download
05/13/05	70 FR 25666	Amendments	National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Direct final rule; amendments.
05/13/05	70 FR 25671	Amendments	National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Proposed rule; amendments.
08/02/01	66 FR 40121	Correction& Amendments	National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Final Rule:Correction and Amendments
08/29/00	65 FR 52587	Amendments	National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Final Rule: Amendments
04/10/00	65 FR 19152	Proposed Rule	National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Proposed Rule
01/05/00	65 FR 452	Notice	Proposed Settlement Agreement/National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production
09/21/98	63 FR 50279	Final Rule	National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production
4/2/97	62 FR 15753	Proposed Rule	Proposal/Public Hearing

NOTES:All files are Government Printing Office (GPO) files unless otherwise indicated.

Closely Related Rules, Policies or Program Guidance

09/21/98

63 FR 50387

Final Rule

Pharaceutical Manufacturing Category Effluent Limitations Guidelines, Pretreatment Standards, and New Source Performance Standards

Other (no files currently available)

Technical Information

Background Information Document (BID)/Response to comments

January 1997	Basis and Purpose Document for the proposed NESHAP for Pharmaceuticals Production
July 1998	Summary of Public Comments and Responses for Final NESHAP for Pharmaceuticals Production (EPA-450/R-98-002)

FACT Sheets

3/20/97

Press Release Fact Sheet

Risk Assessement Information

Implementation Information

Implementation Contacts

Technical and Rule Development Lead:
Randy McDonald, EPA/ESD
mcdonald.randy@epa.gov
Implementation Lead:
Mary Ann Warner, EPA/ITPID
warner.maryann@epa.gov
Enforcement Lead:
Marcia Mia, EPA/OECA
mia.marcia@epa.gov

Implementation Documents

Implementation Tools

	Pharmaceutical MACT Rule Assistant The website provides an electronic expert system designed to identify applicable requirements for your facility
	Using the Pharmaceutical MACT Rule Assistant

Outreach and Training Materials

Permitting Information

1/15/2001

Title V Permit for Merck Sharp and Dohme Quimica
in Barceloneta, Puerto Rico

Compliance and Enforcement Information

9/2001	Inspection Checklist
9/2001	How To Use The Checklist
	EPA document 305-B-04-001-MACT Case Studies
8/26/03	Compliance Assistance Tool	WPD format	PDF format

Pharmaceuticals Production Sector Notebook. Sector notebooks are developed by EPA's Office of Enforcement and Compliance Assurance (OECA)and contain multimedia information (air, water, and land pollutant release data) for a specific industry.

Other

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