OMB.report

Federal forms, ICRs, and supporting documents

Information Collection Request

Survey of Rapid Influenza Diagnostic Test (RIDT) Practices in Laboratories

ICR 201112-0920-005 · OMB 0920-0924 · Historical Active

Forms and Documents
DocumentTypeStatusAvailability
Rapid Influenza Diagnostic Testing Practices in Laboratories Form New Available
Supporting Statement B lw2 rev.docx Supporting Statement B Uploaded 2011-12-08 Available
Attachment J Cover letter lw2 for the survey.doc Supplementary Document Uploaded 2011-12-08 Available
Attachment I Phone script for reminder calls.doc Supplementary Document Uploaded 2011-12-08 Available
Attachment B 60-day FRN.pdf Supplementary Document Uploaded 2011-12-08 Available
Attachment A Authorizing legislation 42USC241.pdf Supplementary Document Uploaded 2011-12-08 Available
Supporting Statement A lw2 rev.docx Supporting Statement A Uploaded 2011-12-08 Available
IC Document Collections
IC IDCollectionTypeStatusForm
200422 Rapid Influenza Diagnostic Testing Practices in Laboratories Form New
ICR Details
0920-0924 201112-0920-005
Historical Active
HHS/CDC
Survey of Rapid Influenza Diagnostic Test (RIDT) Practices in Laboratories
New collection (Request for a new OMB Control Number)   No
Regular
Approved without change 02/22/2012
Retrieve Notice of Action (NOA) 12/12/2011
  Inventory as of this Action Requested Previously Approved
02/28/2013 12 Months From Approved
2,040 0 0
1,020 0 0
0 0 0
Thisis a national systematic study investigating RIDT practices in clinical laboratories. RIDT are the only influenza tests that can provide results while the patient is present in facility, thus the appropriate use of the tests and interpretation of the results is critical to the treatment and control of influenza. Understanding the use of RIDT and how the labs report results to emergency and health departments and treatment facilities and what quality assurance practices are used will guide efforts of CDC to develop influenza testing guidelines and training materials for clinicians.
US Code: 42 USC 241 Name of Law: Public Health and Welfare
  
None
Not associated with rulemaking
  76 FR 33303 06/08/2011
76 FR 76736 12/08/2011
Yes
1
IC Title Form No. Form Name
Rapid Influenza Diagnostic Testing Practices in Laboratories none Rapid Influenza Diagnostic Testing Practices in Laboratories
  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 2,040 0 0 2,040 0 0
Annual Time Burden (Hours) 1,020 0 0 1,020 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
This is a new ICR.
$65,184
Yes Part B of Supporting Statement
No
No
No
No
Uncollected
Daniel Holcomb 770 488-4472 [email protected]
  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.
12/12/2011