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.