In accordance
with 5 CFR 1320, the information collection is approved for a
period of one year. Upon resubmission to OMB, the agency must
provide a summary of all comments made on the information
collection - in addition to a summary of all changes made in
response to these comments. Furthermore, the agency should reduce
or eliminate redundant collection of information from principal
investigators that share laboratory facilities and reduce the
burden associated with amending registrations by limiting the
information required from respondents to changes in their
registration/application.
Inventory as of this Action
Requested
Previously Approved
05/31/2005
05/31/2005
05/31/2004
9,801
0
9,801
25,460
0
25,460
0
0
0
Information to determine that persons
seeking to register have a lawful purpose to posses, use, or
transfer agents or toxins will also be requested as part of the
registration process.
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.