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Toxic Chemical Release Inventory Reporting Forms and Instructions

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Appendix C<br />

1998, <strong>and</strong> subsequently revises only one chemical<br />

submission, the facility will receive a FDP for<br />

<strong>Reporting</strong> Year 1998 with only the revised chemical<br />

included in the <strong>Chemical</strong> Reports section. Hence<br />

there may be fewer chemical reports than chemicals<br />

listed in the <strong>Chemical</strong> Summary section. If only<br />

facility level changes have occurred (i.e., Part I of the<br />

Form R or A), this section is not provided.<br />

B. Levels of Errors Identified in FDPs:<br />

Notice of Non-Technical Data Change<br />

(NDC), Notice of Technical Errors<br />

(NOTE), Notice of Significant Errors<br />

(NOSE). Notice of Noncompliance (NON).<br />

FDP Error <strong>Reporting</strong>. In addition to “echoing back” the<br />

information a facility has submitted, FDPs are used to identify<br />

potential errors, as well as indicate where the TRI Data<br />

Processing Center has made minor clerical changes to<br />

submissions. As submission information is entered into EPA’s<br />

national database, a series of automated data quality checks are<br />

performed. The data quality checks are useful to identify<br />

potential errors with certain data fields such as TRI Facility<br />

Identification, facility name, county spelling, as well as to<br />

perform validation checks to ensure consistency among data<br />

elements within a given Form R or Form A. These data quality<br />

checks, however, cannot detect whether release, transfer, or<br />

waste management quantities were calculated or entered<br />

accurately. Within a FDP notice, there may be up to three<br />

different types of errors identified.<br />

First, a Non-Technical Data Change (NDC) notifies you of<br />

simple, clerical errors that the TRI Data Processing Center has<br />

corrected for you. It is not necessary to respond to a NDC.<br />

The TRI Data Processing Center will correct simple, clerical<br />

errors that are not technical or scientific — a “non-technical<br />

data change.” For example, if a facility transposes CAS<br />

numbers (e.g., the submitter lists 7623-00-0 for sodium nitrite<br />

instead of 7632-00-0), the TRI Data Processing Center will<br />

correct this clerical error <strong>and</strong> display the correct information on<br />

the facility’s FDP. If a facility lists a specific glycol ethers<br />

subcategory, the TRI Data Processing Center will replace this<br />

subcategory with the reportable name “certain glycol ethers.”<br />

The messages used on FDPs to report non-technical data<br />

changes are shown at the end of this appendix under the<br />

heading “E. Messages Used to Report Notices of Technical<br />

Errors (NOTEs) <strong>and</strong> Non-technical Data Changes (NDCs).”<br />

Second, a Notice of Technical Error (NOTE) highlights<br />

inconsistencies or miscalculations that may distort your<br />

facility’s information in EPA’s public data products or skew<br />

analyses. Incomplete addresses, no technical or public contact<br />

provided, missing or invalid SIC codes, or the use of range<br />

codes to report PBT chemical releases are all examples of<br />

technical errors. You should respond to NOTEs as soon as<br />

possible. These types of errors require that the reporting<br />

facility make corrections on its FDP (or provide the TRI Data<br />

Processing Center with a brief explanation why they do not<br />

believe that it is an error) or submit a revised Form R or Form<br />

A. Depending upon when your changes are received, there<br />

may or may not be sufficient time to incorporate them into<br />

EPA’s database in time for public data release. Technical<br />

errors do not prevent submissions from being entered into the<br />

data management system, but indicate inconsistencies or<br />

miscalculations in the submitted form. These errors can<br />

distort public information products <strong>and</strong> skew any analyses if<br />

not corrected. The messages used on FDPs to report NOTEs<br />

are shown below at the end of this appendix under the heading<br />

“E. Messages Used to Report Notices of Technical Errors<br />

(NOTEs) <strong>and</strong> Non-technical Data Changes (NDCs).”<br />

Third, more serious errors are classified as Notices of<br />

Significant Errors (NOSE). The FDP contains the Notice of<br />

Significant Error if applicable. Significant errors prevent<br />

submissions from being entered into the TRI Data Processing<br />

Center data management system or do not allow the TRI Data<br />

Processing Center to verify the authenticity of the submission.<br />

Invalid forms, missing pages, no certification signature, no<br />

chemical name or CAS number are examples of significant<br />

errors. These types of errors require that the reporting facility<br />

make corrections on their FDP, submit a revised Form R or<br />

Form A, or provide the TRI Data Processing Center with a<br />

brief explanation why they do not believe that it is an error.<br />

A facility must respond to a Notice of Significant Error within<br />

21 days of receipt. Failure to respond within the initial 21 day<br />

requirement could result in the issuance of a Notice of<br />

Noncompliance (NON). A Notice of Noncompliance is not<br />

included in a FDP <strong>and</strong> is mailed separately.<br />

The Agency will issue a conditional Notice of<br />

Noncompliance (NON) to a facility for failure to respond to<br />

a Notice of Significant Error (NOSE) within the required<br />

period. A NON will require a facility to take the corrective<br />

action noted in the NOSE within 21 days <strong>and</strong> respond to the<br />

Agency that corrective action has been taken. If a facility fails<br />

to respond to the NON within the required time period, the<br />

Agency may take further action.<br />

Facilities must keep copies, for three years, of submitted Form<br />

R reports <strong>and</strong> Form A certifications <strong>and</strong> all documentation<br />

used to complete their submissions. This documentation<br />

should include calculations for threshold determinations, the<br />

basis of exemptions applied, <strong>and</strong> the estimation techniques<br />

<strong>and</strong> data used for all quantities reported on the Form R <strong>and</strong><br />

Form A.<br />

C–2 <strong>Toxic</strong>s <strong>Release</strong> <strong>Inventory</strong> <strong>Reporting</strong> <strong>Forms</strong> <strong>and</strong> <strong>Instructions</strong>

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