Generic Clearance to Conduct Formative Research/CNPP

Forms and Documents

Document Name	Status
APPENDIX 11_2015 - 2020 Dietary Guidelines for Americans.pdf Supplementary Document	2019-09-13
APPENDIX 10_Sample Participant Screener.pdf Supplementary Document	2019-09-13
APPENDIX 9_Sample Confidentiality Agreement.pdf Supplementary Document	2019-09-13
APPENDIX 8_Legal Authority - Government Performance and Results Act of 1993.pdf Supplementary Document	2019-09-13
APPENDIX 7_Legal Authority - National Nutrition Monitoring & Related Research Act of 1990.pdf Supplementary Document	2019-09-13
APPENDIX 6_Legal Authority - National Agriculture Research, Extension, & Teach Policy Act of 1977.pdf Supplementary Document	2019-09-13
Generic Clearance_OMB 0584-0523 9.24.19 clean version.docx Supporting Statement A	2019-09-24

IC Document Collections

IC ID	Document Title	Status
242953	DGA 2020-2025 Survey and Focus Group (English and Spanish) Other-Attachment C-1 Screener (English) (B-24 Caregiver Audience	New

ICR Details

OMB Control No: 0584-0523	ICR Reference No: 201902-0584-002
Status: Active	Previous ICR Reference No: 201601-0584-002
Agency/Subagency: USDA/FNS	Agency Tracking No: Renewal
Title: Generic Clearance to Conduct Formative Research/CNPP
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 11/20/2019
	Date Received in OIRA: 09/26/2019
Terms of Clearance: This generic ICR umbrella s approved on the understanding that: 1) ICs under this generic clearance will not overlap with ICs under other FNS generic clearances; 2) to the extent that FNS and FDA both conduct studies related to MyPyramid and/or the Dietary Guidelines, FNS and FDA will coordinate their IC activities and share information with each other so as not to duplicate ICs and impose unnecessary burden on the public; 3) respondents will not be asked to respond to these ICs more than quarterly; 4) CNPP will continue to use screening measures when conducting random sampling to ensure that individual members of the public are not included in multiple studies within designated periods of time; 5) because it is unclear if FNS has the statutory authority to provide assurances of confidentiality, FNS will not use the term "confidential" in any materials provided to respondents and will instead use terms like "private to the extent permitted by law"; 6) FNS will submit individual ICs to OMB, along with all necessary supporting statements and burden estimates. OMB will aim to conclude review within 14 days. However, FNS should not assume individual ICs have received OMB approval until FNS has received such approval explicitly, even after 14 days have elapsed.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	11/30/2022	36 Months From Approved	11/30/2019
Responses	174,300	0	57,000
Time Burden (Hours)	37,065	0	12,004
Cost Burden (Dollars)	0	0	0

---

Abstract: Information collection is necessary to obtain input from individuals in the public in order to develop useful educational messages and materials in the support of the Dietary Guidelines for Americans and MyPyramid.

---

Authorizing Statute(s): US Code: 7 USC 5341 Name of Law: National Nutrition Monitoring and Related Research Act of 1990
   US Code: 31 USC 9701 Name of Law: Government Perforamcne and Results Act of 1993
   US Code: 7 USC 3171-3175 Name of Law: National Agriculture Research, Extension, and Teach Policy Act of 1977
  

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:
	84 FR 66	04/05/2019
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 50372	09/25/2019
Did the Agency receive public comments on this ICR? Yes

---

Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
DGA 2020-2025 Survey and Focus Group (English and Spanish)

---

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	174,300	57,000	0	0	117,300	0
Annual Time Burden (Hours)	37,065	12,004	0	0	25,061	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

---

Annual Cost to Federal Government: $6,167

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

---

Common Form ICR:  No

---

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: 09/26/2019

---