Final Rule Alert: EPA Updates Risk Management Program for Chemical Facilities
UPDATE: US EPA on May 30, 2018 published a proposed rule to “rescind almost all the requirements added to the accident prevention provisions program” of a 2017 rulemaking that expanded the Clean Air Act Risk Management Plan (RMP)chemical accident prevention requirements.
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On December 21, EPA Administrator Gina McCarthy signed a Final Rule to amend the Clean Air Act Risk Management Plan (RMP) requirements for chemical facilities.
1. Require all facilities with Program 2 or 3 processes to conduct a root cause analysis as part of an incident investigation into a catastrophic release or a near-miss;
2. Require regulated facilities with a Program 2 or 3 processes to contract with an independent third party to perform a compliance audit after the facility has a reportable release; and
3. Require owners or operators of facilities with Program 3 processes under NAICS Codes 322 (paper manufacturing), 234 (petroleum and coal products manufacturing) and 325 (chemical manufacturing) to add a safer technology and alternatives analysis (STAA) to its process hazard analysis (PHA).
A pre-publication copy of the Final Rule is available here.
1. Require owners/operators of facilities with Program 2 or 3 processes to coordinate with local emergency response agencies at least once per year to ensure preparedness to respond to an accidental release of a regulated substance;
2. Require facilities with Program 2 or 3 processes to conduct annual notification exercises to ensure emergency contact information is accurate and complete;
3. Require all facilities subject to the emergency response pre-program requirements (Subpart E) to conduct a full field exercise at least once every ten years and tabletop exercises at least once every three years.
In the proposed rule, published in the Federal Register in March 2016, EPA put forth requirements for facilities to provide certain information to emergency responders. In the Final Rule, EPA instead will require facilities to share information during annual coordination activities between the facility and responders.
Build the expertise needed to make informed on-the-job decisions that help your site control pollution, prevent releases, and maintain compliance with US EPA’s Clean Air Act rules. The Clean Air Act Regulations guides professionals through compliance with Title V permit requirements, emissions and pollution controls, annual greenhouse gas (GHG) reporting, Risk Management Planning (RMP) responsibilities, and more.
Interactive, easy to use, and available 24/7, the new online course will help you get up to speed with new and changing EPA clean air rules and protect your facility from costly EPA enforcement.
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On December 21, EPA Administrator Gina McCarthy signed a Final Rule to amend the Clean Air Act Risk Management Plan (RMP) requirements for chemical facilities.
Clean Air Act RMP Accident Prevention Program Revisions
The Final Rule includes three revisions to the accident prevention program requirements under the RMP:1. Require all facilities with Program 2 or 3 processes to conduct a root cause analysis as part of an incident investigation into a catastrophic release or a near-miss;
2. Require regulated facilities with a Program 2 or 3 processes to contract with an independent third party to perform a compliance audit after the facility has a reportable release; and
3. Require owners or operators of facilities with Program 3 processes under NAICS Codes 322 (paper manufacturing), 234 (petroleum and coal products manufacturing) and 325 (chemical manufacturing) to add a safer technology and alternatives analysis (STAA) to its process hazard analysis (PHA).
A pre-publication copy of the Final Rule is available here.
Clean Air Act RMP Emergency Response “Enhancements”
The Final Rule includes three “enhancements” to bolster the requirements for RMP emergency preparedness and response. The RMP emergency response enhancements are as follows:1. Require owners/operators of facilities with Program 2 or 3 processes to coordinate with local emergency response agencies at least once per year to ensure preparedness to respond to an accidental release of a regulated substance;
2. Require facilities with Program 2 or 3 processes to conduct annual notification exercises to ensure emergency contact information is accurate and complete;
3. Require all facilities subject to the emergency response pre-program requirements (Subpart E) to conduct a full field exercise at least once every ten years and tabletop exercises at least once every three years.
Enhanced Clean Air Act RMP Information Availability
Lastly, the Final Rule sets requirements to make chemical hazard information more easily available to the public. Among these enhancements is a requirement for the facility owner or operator to provide ongoing notification of information availability on a company website, social media, or other publicly accessible place. If and when an RMP reportable accident occurs, the facility must hold a public meeting within 90 days of the incident.In the proposed rule, published in the Federal Register in March 2016, EPA put forth requirements for facilities to provide certain information to emergency responders. In the Final Rule, EPA instead will require facilities to share information during annual coordination activities between the facility and responders.
New Clean Air Act Online Course Now Available!
Build the expertise needed to make informed on-the-job decisions that help your site control pollution, prevent releases, and maintain compliance with US EPA’s Clean Air Act rules. The Clean Air Act Regulations guides professionals through compliance with Title V permit requirements, emissions and pollution controls, annual greenhouse gas (GHG) reporting, Risk Management Planning (RMP) responsibilities, and more.
Interactive, easy to use, and available 24/7, the new online course will help you get up to speed with new and changing EPA clean air rules and protect your facility from costly EPA enforcement.
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