Approved with the understanding that, upon approval, FDA will discontinue OMB control number 0910-0755, which currently accounts for 104,679 responses and 108,392 hours associated with recordkeeping requirements in 21 CFR part 56.
table that charts list comparision
Inventory as of this Action
Requested
Previously Approved
01/31/2023
36 Months From Approved
06/30/2020
346,800
0
36,792
1,731,430
0
3,679,200
147,171,550
0
0
The information collection supports FDA regulations governing Institutional Review Boards and the rights and welfare of human subjects involved in FDA-regulated research. Respondents to the collection are sponsors, members, or other individuals subject to the requirements of 21 CFR parts 50 and 56..
US Code:
42 USC 289
Name of Law: Public Health and Welfare; Institutional Review Boards
US Code:
21 USC 301 et. seq.
Name of Law: Federal Food, Drug, and Cosmetic Act
The information collection reflects both changes and adjustments. We revised the information collection to consolidate it with control no. 0910-0755. In this request, our estimate reflects a decrease in the average number of annual responses by 1,947,770, but an increase in the average number of annual hours by 310,008.
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.