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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View ICR - OIRA Conclusion
OMB Control No:
0910-0543
ICR Reference No:
200705-0910-001
Status:
Historical Active
Previous ICR Reference No:
200404-0910-004
Agency/Subagency:
HHS/FDA
Agency Tracking No:
Title:
Eligibility Determination for Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)
Type of Information Collection:
Extension without change of a currently approved collection
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved with change
Conclusion Date:
08/17/2007
Retrieve Notice of Action (NOA)
Date Received in OIRA:
05/01/2007
Terms of Clearance:
Please note burden table amended to reflect agency adjustment rather than program changes.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
08/31/2010
36 Months From Approved
08/31/2007
Responses
5,848,435
5,848,435
1,274,272
Time Burden (Hours)
3,086,115
3,086,115
866,240
Cost Burden (Dollars)
0
0
0
Abstract:
Under section 361 of the Public Health Service Act (the PHS Act) (42 U.S.C. 264), FDA may issue and enforce regulations necessary to prevent the introduction, transmission, or spread of communicable diseases between the States or possessions or from foreign countries into the States. As derivatives of the human body, all HCT/Ps pose some risk of carrying pathogens that could potentially infect recipients or handlers. FDA has issued regulations related to HCT/Ps involving establishment registration and listing using Form FDA 3356; eligibility determination for donors; and current good tissue practice (CGTP). Form FDA 3356: Establishment Registration and Listing for Human Cells, Tissues, and Cellular and Tissue-Based Products is used to submit the required information (???? 1271.10, 1271.21, 1271.25, and 1271.26).
Authorizing Statute(s):
US Code: 42 USC 264 Name of Law: Public Health Service Act
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
72 FR 3858
01/26/2007
30-day Notice:
Federal Register Citation:
Citation Date:
72 FR 21027
04/27/2007
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
27
IC Title
Form No.
Form Name
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
Establishment Registration and Listing; Form FDA 3356; Eligibility Determination for Donors; and Current Good Tissue Practice
FDA-3356, FDA-3356
FDA-3356
,
FDA-3356
ICR Summary of Burden
Total Approved
Previously Approved
Change Due to New Statute
Change Due to Agency Discretion
Change Due to Adjustment in Estimate
Change Due to Potential Violation of the PRA
Annual Number of Responses
5,848,435
1,274,272
0
0
4,574,163
0
Annual Time Burden (Hours)
3,086,115
866,240
0
0
2,219,875
0
Annual Cost Burden (Dollars)
0
0
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
Yes
Burden Increase Due to:
Miscellaneous Actions
Burden decreases because of Program Change due to Agency Discretion:
Yes
Burden Reduction Due to:
Miscellaneous Actions
Short Statement:
The 2004 burden estimate for 0910-0543 was 866,240. The increase in burden to 3,086,113.65 is attributed to the consolidation of OMB packages: 0910-0469 and 0910-0559 and an increase in the number of establishments as well as total annual responses and records based on updated information since the issuance of the Eligibility Determination for Donors of HCT/Ps and CGTP final rules.
Annual Cost to Federal Government:
$3,378,622
Does this IC contain surveys, censuses, or employ statistical methods?
No
Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002?
No
Is this ICR related to the Affordable Care Act [PPACA, P.L. 111-148 & 111-152]?
Uncollected
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
Uncollected
Agency Contact:
Saleda Perryman
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:
(a) It is necessary for the proper performance of agency functions;
(b) It avoids unnecessary duplication;
(c) It reduces burden on small entities;
(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;
(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;
(f) It indicates the retention periods for recordkeeping requirements;
(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:
(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;
(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.
(i) It uses effective and efficient statistical survey methodology (if applicable); and
(j) It makes appropriate use of information technology.
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.
Certification Date:
05/01/2007
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