What is CAA 112r?
What is CAA 112r?
The General Duty Clause (GDC) CAA Section 112(r)(1), directs owners and operators of stationary sources to identify hazards that may result from accidental releases, to design and maintain a safe facility, and to minimize the consequences of releases when they occur.
What triggers RMP?
The RMP rule requires facilities that use extremely hazardous substances to develop a Risk Management Plan which: identifies the potential effects of a chemical accident, identifies steps the facility is taking to prevent an accident, and. spells out emergency response procedures should an accident occur.
How do I submit an RMP?
NOTE: If this is the first time an RMP is being submitted for your facility you do not need a facility ID#.
- Step 1: Register the Certifying Official in CDX.
- Step 2: Complete the Electronic Signature Agreement (ESA) and mail it to EPA.
- Step 3: Register the “Preparer” and activate RMP*eSubmit access in CDX.
What is the purpose of a CAA risk management plan?
Section 112(r) of the Clean Air Act (CAA) requires covered facilities to develop risk management programs to prevent accidental releases of dangerous chemicals. Facilities are required to submit risk management plans (RMPs) to a central location by June 1999.
What is Cal ARP?
CalARP is the Federal Risk Management Plan Program with additional state requirements, including an additional list of regulated substances and thresholds. The federal regulations are found in Code of Federal Regulations (CFR), Title 40, Part 68.
When should I update my RMP?
RMPs must be updated at least once every five years. Owners and operators responsible for RMP implementation should review A Checklist for Submitting your Risk Management Plan (RMP). You may use RMP*eSubmit for your resubmission.
What is RMP in pharmaceutical jurisprudence?
Registered Medical Practitioner (RMP) means Medical Practitioner whose name appear on the official register kept for the purpose in accordance with the law of the land to which one belongs.