Air Toxics Website: Rule and Implementation Information for Pharmaceuticals Production Industry
(Docket# A-96-03
From the listing below, find the file you would like to download.
Rule Information
Proposed and Promulgated Rules
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
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