Requirements for the Importation of Nonhuman Primates into the United States

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 7510A Application for Registration as an Importer of Nonhuman Primates	Form and Instruction	Unchanged	Available
Form 75.10A Attachment C - CDC 75.10A Application for Registration as an Importer of...	Form	Unchanged	Available
Form 75.10 Attachment E - CDC PGA Message Set Requested Data of Live Nonhuman Prima...	Form	Unchanged	Available
Form 71.53 Documentation of Non - Infectionusness	Form and Instruction	Unchanged	Available
Form 71.53 CDC Partner Government Agency Message Set for Importing Nonhuman Primates	Form and Instruction	Unchanged	Available
Form 71.53(v) (No Form) Filovirus Diagnostic Specimen Submission Form for Non-human Primate Materials	Form and Instruction	Unchanged	Available
Form 71.53(n) (no form) Recordkeeping and reporting requirements for importing Nonhuman primates	Form and Instruction	Unchanged	Available
Form 71.53(g)(1)(iii) Attachment E - CDC PGA Message Set Requested Data of Live Nonhuman Prima...	Form and Instruction	Unchanged	Repair queued
0920-0263 ITDS Nonsub_RC ir.docx	Justification for No Material/Nonsubstantive Change	Uploaded 2016-11-16	Available
Attachment A5 - 49 CFR part 1520.11(b).pdf	Supplementary Document	Uploaded 2014-06-19	Available
Attachment A2 - 42 CFR part 71 Foreign Quarantine.pdf	Supplementary Document	Uploaded 2014-06-19	Available
Attachment A1 - Section 361 Public Health Service Act (42 USC 264).pdf	Supplementary Document	Uploaded 2014-06-19	Available
0920-0263 Revision ITDS Supptg Stmt B.docx	Supporting Statement B	Uploaded 2014-06-19	Available
0920-0263 Revision ITDS SUPPTG STMT A.docx	Supporting Statement A	Uploaded 2014-06-19	Available
Attachment 3 Special Permit Procedure.pdf	Supplementary Document	Uploaded 2013-02-21	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
6722	Importer Registration and New Importer Registration - Nonhuman Primates	Form and Instruction	Unchanged	Application for Registration as an Importer of Nonhuman Primates
212043	Nonhuman Primate Importer Application for Registration as an Importer of Nonhuman Primates (New Importer)	Form	Unchanged	Attachment C - CDC 75.10A Application for Registration as an Importer of...
212042	Nonhuman Primate Importer Recordkeeping and reporting	Form	Unchanged	Attachment E - CDC PGA Message Set Requested Data of Live Nonhuman Prima...
212007	Documentation of Non-infectiousness	Form and Instruction	Unchanged	Documentation of Non - Infectionusness
212006	Importer/Filer	Form and Instruction	Unchanged	CDC Partner Government Agency Message Set for Importing Nonhuman Primates
206055	Filovirus Diagnostic Specimen Submission	Form and Instruction	Unchanged	Filovirus Diagnostic Specimen Submission Form for Non-human Primate Materials
206054	Quarantine Release	Other-Data Elements	Unchanged
206053	Recordkeeping and Reporting Requirements for importing Nonhuman Primates	Form and Instruction	Unchanged	Recordkeeping and reporting requirements for importing Nonhuman primates
206052	Documentation and Standard Operating Procedures (No Form)	Form and Instruction	Unchanged	Attachment E - CDC PGA Message Set Requested Data of Live Nonhuman Prima...

ICR Details

OMB Control No: 0920-0263	ICR Reference No: 201611-0920-007
Status: Historical Active	Previous ICR Reference No: 201406-0920-013
Agency/Subagency: HHS/CDC	Agency Tracking No: 17EP
Title: Requirements for the Importation of Nonhuman Primates into the United States
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 11/17/2016
Retrieve Notice of Action (NOA)	Date Received in OIRA: 11/16/2016
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2017	09/30/2017	09/30/2017
Responses	5,187	0	5,187
Time Burden (Hours)	943	0	943
Cost Burden (Dollars)	0	0	0

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Abstract: Request to change the method for respondents to submit forms; forms can be submitted via the International Trade Data System and the Automated Cargo Environment. There is no change in burden or forms.

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Authorizing Statute(s): US Code: 42 USC 264 Name of Law: Regulations to Control Communicable Diseases
   US Code: 19 USC 1411 Name of Law: Tariff Act of 1930 (As amended by the Safe Port Act of 2006)
   EO: EO 13659 Name/Subject of EO: Streamlining the Export/Import Process for America's Businesses
  

Citations for New Statutory Requirements: US Code: 42 USC 71 Name of Law: The Public Health and Welfare

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 15129	03/18/2014
30-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 33924	06/13/2014
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 9

table that charts list of burden

IC Title	Form No.	Form Name
Documentation and Standard Operating Procedures (No Form)	71.53(g)(1)(iii)	Attachment E - CDC PGA Message Set Requested Data of Live Nonhuman Prima...
Documentation of Non-infectiousness	71.53	Documentation of Non - Infectionusness
Filovirus Diagnostic Specimen Submission	71.53(v) (No Form)	Filovirus Diagnostic Specimen Submission Form for Non-human Primate Materials
Importer Registration and New Importer Registration - Nonhuman Primates	7510A	Application for Registration as an Importer of Nonhuman Primates
Importer/Filer	71.53	CDC Partner Government Agency Message Set for Importing Nonhuman Primates
Nonhuman Primate Importer Application for Registration as an Importer of Nonhuman Primates (New Importer)	75.10A	Attachment C - CDC 75.10A Application for Registration as an Importer of...
Nonhuman Primate Importer Recordkeeping and reporting	75.10	Attachment E - CDC PGA Message Set Requested Data of Live Nonhuman Prima...
Quarantine Release
Recordkeeping and Reporting Requirements for importing Nonhuman Primates	71.53(n) (no form)	Recordkeeping and reporting requirements for importing Nonhuman primates

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ICR Summary of Burden

table that charts list 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	5,187	5,187	0	0	0	0
Annual Time Burden (Hours)	943	943	0	0	0	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: CDC is requesting the following changes based on the upcoming implementation of ITDS and ACE, which allows NHP importers/filers to voluntarily submit data concerning CDC-regulated imports electronically to CBP for clearance. These estimates are based on operational observation by Quarantine Staff at US ports of entry. • 150 submissions of CDC PGA Message Set importing Live Nonhuman Primates, resulting in 38 additional requested burden hours • 2280 submissions of CDC PGA Message Set data for importations of Nonhuman Primate products, resulting in an additional 570 requested burden hours • 2280 submissions of documentation indicating that Nonhuman Primate products have been rendered noninfectious, resulting in an additional 190 hours of requested burden. These submissions can be accomplished via the Document Imagining System. CDC retains the right to collect these in hard copy. The following change is a correction to clarify the public burden associated with providing the required statements and documentation that an NHP product has been rendered non-infectious. • 2280 submissions of documentation indicating that Nonhuman Primate products have been rendered noninfectious, resulting in an additional 190 hours of requested burden. These submissions can be accomplished via the Document Imagining System. CDC retains the right to collect these in hard copy. The estimates provided in this information collection request assume that every commercial importer of NHP covered by CDC's regulations will file a data entry using ITDS and ACE. However, CDC is maintaining its authority to collect hard copies of required documentation, as currently authorized by the Office of Management and Budget, because the use of ITDS/ACE will not be required for imports entering the United States until a later date. CDC will accept both hard copy and electronic filing of import-related documentation until the use of ACE is required for cargo entering the United States.

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Annual Cost to Federal Government: $433,788

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

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 [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

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Common Form ICR:  No

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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: 11/16/2016

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