Technology Transfer Network - Air Toxics Web Site
Air Toxics Website: Rule and Implementation Information for Pharmaceuticals Production Industry
On this page:
Rule Information
Proposed and Promulgated Rules
Subpart GGG - National Emission Standards for Pharmaceuticals Production
| Date | Citation | Action | Description | File Download |
| 04/21/2011 | 76 FR 22566 | Final Rule | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production. Final Rule, Residual Risk and Technology Review. |  696 kb |
| 10/21/2010 | 75 FR 65067 | Proposed Rule | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production. Proposed Rule, Residual Risk and Technology Review. | 599 kb |
05/13/2005 | 70 FR 25666 | Amendments | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Direct final rule; amendments. | |
| 05/13/2005 | 70 FR 25671 | Amendments | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Proposed rule; amendments. | |
| 08/02/2001 | 66 FR 40121 | Correction& Amendments |
National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Final Rule:Correction and Amendments | |
| 08/29/2000 | 65 FR 52587 | Amendments | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Final Rule: Amendments | |
| 04/10/2000 | 65 FR 19152 | Proposed Rule | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production-Proposed Rule | |
| 01/05/2000 | 65 FR 452 | Notice | Proposed Settlement Agreement/National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production | |
| 09/21/1998 | 63 FR 50279 | Final Rule | National Emission Standards for Hazardous Air Pollutants for Pharmaceuticals Production | |
| 4/2/1997 | 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 | |
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 | |
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
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 |  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.
NOTE: Most
links on this page are pointers to other hosts and locations in the Internet.
This information is provided as a service; however the U.S. Environmental
Protection Agency does not endorse, approve or otherwise support these
sites.