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OAR Policy and Guidance Metarecord

Document Title/Subject:
Pharmaceuticals Production: Air Toxics Proposed Rule
Related Documents:
Signed by: Christine Todd Whitman

Signature Date: July 24, 2001

Contact:
Randy McDonald
(919) 541-5402

Filename(s):
http://www.epa.gov/ttn/oarpg/t3/fr_notices/pharm_fr.pdf
URL(s):

 

Regulatory Authority:
Title 3
Division/Director:
Emission Standards Division (OAQPS) / Sally Shaver
Submitted By:
noell.maria
OGC Contact:
Karen Clark
OGC Phone#:
202-564-5477
Internet Contact:
Jeff Clark
Document Type:
Proposed & Final Preambles & Rules,
EPA Document Number:

Federal Register:
Supersedes:
Subject Category:
AIR
ENVIRONMENTAL PROTECTION AGENCY
Keywords:
Emissions
Hazardous air pollutants
HAPs
Maximum Achievable Control Technology Emission Standards
MACTs
National Emission Standards for Hazardous Air Pollutants
NESHAPs
Pollutants
Pharmaceuticals Production
Terms:
Air pollutants
Clean Air Act
CAA
Standards
Abstract:
The EPA is proposing to amend the NESHAP for pharmaceuticals production. This action proposes to correct referencing errors, add test methods for analyzing wastewater, define triethylamine as a soluble hazardous air pollutant (HAP) instead of a partially soluble HAP, add an outlet concentration limit for storage tank emissions, clarify the monitoring frequency requirements for connectors, and add planned routine maintenance provisions for centralized combustion control devices. This file is the text of the parallel proposal.

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