Pursuant to the
PRA and 5 CFR 1320 this collection of information is approved for
three years with the exception noted below. The preamble to the
final rule treats information provided by the NRC and NIH as
petitions for reconsideration and establishes a 60 day comment
period for the purposes of receiving additional information. The
preamble also implements a 3 month stay of Subpart I to provide
time to assess the information provided and whether further
rulemaking action is needed. Therefore, the information collection
associated with Subpart I is not approved at this time. When (and
if) the agency submits Subpart I for PRA review, it should clearly
demonstrate that the information required: (1) does not duplicate
information otherwise available to EPA, (2) is the least burdensome
necessary to carry out agency objectives, and (3) has practical
utility.
Inventory as of this Action
Requested
Previously Approved
11/30/1992
11/30/1992
196
0
0
40,554
0
0
0
0
0
OWNERS OR OPERATORS OF SOURCES OF
RADIONUCLIDES EMITTED TO THE ENVIRONMENT ARE REQUIRED TO
DEMONSTRATE COMPLIANCE WITH EMISSION STANDARDS THROUGH THE CONDUCT
OF TESTS AND CALCULATIONS, AS APPROPRIAT TEST AND CALCULATION
INFORMATION IS SUBMITTED TO EPA. RECORDS ARE KEPT FOR A PERIOD OF
TIME.
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.