Previous terms
continue: OMB approves this collection for a period of three years.
To request approval of information collections under this generic
approval, the agency must do the following: 1) Unless an agency is
using multiple modes of collection (e.g., paper forms and
electronic submissions), provide a Generic Clearance Submission
Template for each Instrument; 2) If the agency is using multiple
modes of collection (e.g., paper forms and electronic submissions),
the same Generic Clearance Submission Template may be used for both
instruments; 3) each Generic Clearance Submission Template must be
uploaded as a Supplementary document using a naming convention that
allows the public to identify the associated instrument; 4) submit
no more than five Generic Submission Templates with each
request.¿
Inventory as of this Action
Requested
Previously Approved
03/31/2016
03/31/2016
03/31/2016
30,750
0
10,250
15,750
0
5,250
0
0
0
This request for nonsubstantive change
is to correct an error made by CDC when the generic ICR was
submitted. The number of responses and burden hours were entered
for one year of information collection, and should have been
tripled to account for the 3 years of clearance.
US Code:
42 USC
41 Name of Law: Public Health Service Act
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.