Data Acquisition for Anticipated Residue and Percent Crop Treated

ICR 200009-2070-003

OMB: 2070-0164

Federal Form Document

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ICR Details
2070-0164 200009-2070-003
Historical Active
EPA/OCSPP
Data Acquisition for Anticipated Residue and Percent Crop Treated
New collection (Request for a new OMB Control Number)   No
Regular
Approved without change 09/07/2001
Retrieve Notice of Action (NOA) 09/28/2000
This ICR covers the activities carried out to meet the requirements under the FQPA of 1996 requiring that tolerance decisions based on anticipated or actual residue (ARs) or percent crop treated (PCT) data to be verified to ensure that residues in or on food are not above the residue levels relied on for establishing the tolerance. It is OMB's understanding that, if EPA relies on anticipated or actual residue levels in establishing, modifying or leaving in effect a tolerance, it must call in data within five years for all crops for which AR's were used for a pesticide. It is understood that EPA may obtain this data by issuing a data call-in. It is also understood that PCT reviews will generally be conducted within the Agency and only in rare instances would a registrant need to gather the information. As such, instead of approving the requested 59 hours for PCT data call-ins, OMB has approved only 1 hour for this activity. Should it become necessary for EPA to seek PCT related data through a data call-in, EPA may submit an Information Collection Worksheet (ICW) to request an adjustment in the total approved hours. The ICW must be submitted and approved by OMB to account for the issuance of the PCT data call-in before it is issued. This collection is approved for three years based on the agreed upon terms of clearance stated below. EPA will not issue any DCI unless the DCI has first been approved by relevant high-level management in the Office of Pesticide Programs, i.e., the directors or deputy directors of the division(s) responsible for requesting the particular studies. Before EPA can issue a specific DCI under this ICR, EPA must use one of the following approaches to provide notice and an opportunity for OMB to review the DCI: (1) Prospective Report. To obtain prior approval for any DCIs that may be planned or anticipated at any point during the approval period for this ICR, EPA should prepare a prospective report that is submitted to OMB as soon as EPA determines that such DCIs are needed. OMB may approve or disapprove any number of the proposed DCIs at the time this report is provided. Furthermore, at any time after the report is submitted to OMB and before the Agency issues the DCI, OMB has the discretion to request that any number of the proposed DCIs included in the prospective report be submitted to OMB on a case by case basis. Finally, these prospective reports should only include those DCIs that are planned or anticipated to occur within 6 months of the submission of the report to OMB. Any DCIs not initiated within the 6 month time frame should be included in a subsequent prospective report. (2) Case-by-case Submissions. If prior approval for the DCI is not obtained as described in (1) above, may submit the individual specific DCI to OMB on a case-by-case basis. Both types of submissions should also contain the following: information about the pesticide, total respondents potentially affected by the DCI, the planned schedule for issuing the DCI and the data due date, the studies to be required, the total costs of the studies, the practical utility of the data, and the estimated paperwork burden and costs related to the DCI, including effects on small businesses (costs should be broken down to include labor and non-labor costs). In its submission to OMB, EPA should also establish grounds for initiating the Data Call-In: ** Under the Special Review Program, EPA should provide a discussion of the evidence used to determine that the use of a particular pesticide may result in "unreasonable adverse effects on the environment" as defined by FIFRA 2(bb). ** Under the Registration Review Program, EPA should provide a discussion of the special circumstances necessitating a collection prior to promulgation of the final rule establishing procedural requirements for that program. It is OMB's understanding that any Registration Review DCI's issued during this approval period would only involve a request for specific information necessary to meet the new statutory requirements established in the Food Quality Protection Act of 1996 which established the Registration Review Program. OMB review of these submissions is expected to be prompt (no more than 15 working days after OMB has confirmed its receipt of the submission); prompt OMB review is more likely where burden is small and practical utility clearly demonstrated. Issues with the DCI -- e.g. lack of transparency or demonstration of compliance with the requirements of 1320.5 (d) may necessitate extended review. OMB may request additional information to help in its determination. OMB may require EPA to publish a Federal Register notice seeking public comment on the DCI and to develop a complete supporting statement for the ICR if the DCI appears highly unusual, controversial, or inconsistent with this clearance. When deciding to require a separate review, OMB will consider the following: (1) total amount of burden/cost and burden/cost per respondent; (2) the number of respondents affected; (3) the degree of similarity (i.e. frequency of use, level of burden and content) with other collections administered under the generic clearance; (4) the evidence of duplication with other collections; and (5) the degree and extent of public concern expected. In addition, the following criteria would also be considered in deciding whether a separate review is appropriate: (1) the environmental and health consequences if the collection is given a separate review and (2) the statutory or judicial deadlines missed if the collection is given a separate review. Note that, because of this second provision, the burden is on EPA to submit supporting material for DCIs as expeditiously as possible. At the end of each 12-month period after the approval of this ICR, EPA must submit a report to OMB that identifies the specific DCIs that were issued under this ICR during that period. Such report should include information about the pesticide, total respondents affected or potentially affected by the DCI, the studies required, the total costs of the studies (including a breakdown of labor vs. non-labor costs based on consultation with respondents), and the estimated paperwork burden and costs related to the DCI. If the aggregate paperwork burden for the DCIs issued during any 12-month period after the approval of this ICR exceeds the estimated annual burden, EPA must submit an ICR Correction Worksheet (ICW) to amend the total annual burden hours in the OMB inventory for this ICR. For future DCI ICR packages, EPA should include as much information as possible about future potential DCIs under this ICR. A more detailed ICR will allow for meaningful public comment and thorough evaluation by OMB, as required in 5 CFR 1320.
  Inventory as of this Action Requested Previously Approved
06/30/2005 06/30/2005
31 0 0
29,807 0 0
0 0 0

This information collection activity will enable EPA's Office of Pesticide Programs (OPP) to obtain information needed to re- evaluate the Agency's original tolerance decisions. The collection and verification of data is necessary to comply with the law. Specifically, Section 408(b)(2)(E)(ii) of FFDCA re- quires data to be called in within five years after each tole- rances decision that relies on anticipated or actual residues; section 408(b)(2)(F)(iv) of FFDCA requires periodic re-evaluation if percent crop treated estimates are used.

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IC Title Form No. Form Name
Data Acquisition for Anticipated Residue and Percent Crop Treated 1911.01

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 31 0 0 31 0 0
Annual Time Burden (Hours) 29,807 0 0 29,807 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
No

$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
09/28/2000


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