National Program of Cancer Registries Cancer Surveillance System (NPCR CSS)

ICR 201304-0920-016

OMB: 0920-0469

Federal Form Document

ICR Details
0920-0469 201304-0920-016
Historical Active 200911-0920-004
HHS/CDC 19239
National Program of Cancer Registries Cancer Surveillance System (NPCR CSS)
Reinstatement with change of a previously approved collection   No
Regular
Approved without change 05/22/2013
Retrieve Notice of Action (NOA) 04/25/2013
  Inventory as of this Action Requested Previously Approved
05/31/2016 36 Months From Approved
96 0 0
192 0 0
0 0 0

CDC's NPCR CSS collects cancer surveillance information from NPCR-funded states and territories regarding the types of cancer that occur (histology, morphology, and behavior), the anatomic location, the extent of disease at the time of diagnosis, the kinds of treatment received by cancer patients, and the outcomes of treatment and clinical management. Continued clearance for a three-year period is requested.

PL: Pub.L. 102 - 515 3312 Name of Law: Cancer Registries Amendment Act
   US Code: 42 USC 241 Name of Law: Public Health Service Act
   PL: Pub.L. 111 - 5 VII Name of Law: American Recovery and Reinvestment Act
  
None

Not associated with rulemaking

  77 FR 73469 12/10/2012
78 FR 22884 04/17/2013
No

  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 96 0 0 96 0 0
Annual Time Burden (Hours) 192 0 0 192 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
There are no changes to the number of respondents or the estimated burden per response. The frequency of reporting will change from annual to semi-annual. The additional report will allow CDC to produce early estimates of cancer incidence and other statistics, in advance of the detailed data validation steps required for final reports. The estimated annualized burden will increase as a result of the increase in the frequency of data collection. This Reinstatement request divides the 48 respondents (central cancer registries) into two groups: a group of 38 respondents that will submit a standard report (Attachment 3a), and a group of 10 respondents that will submit an enhanced report which includes additional variables (Attachment 3b). However, since the data files are electronically created, there is no additional burden associated with including the additional variables in the electronic data file (report). The estimated burden per response is 2 hours and is the same for both groups of respondents.

$1,720,955
Yes Part B of Supporting Statement
No
No
No
Yes
Uncollected
Catina Conner 4046394775

  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.
04/25/2013


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