IMPORTATION AND SHIPMENT OF ETIOLOGIC AGENTS

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
110849	IMPORTATION AND SHIPMENT OF ETIOLOGIC AGENTS	Form	Migrated

ICR Details

OMB Control No: 0920-0199	ICR Reference No: 198903-0920-001
Status: Historical Active	Previous ICR Reference No: 198703-0920-001
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: IMPORTATION AND SHIPMENT OF ETIOLOGIC AGENTS
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 06/06/1989
	Date Received in OIRA: 03/09/1989
Terms of Clearance: This information collection request was submitted pursuant to a reques for all collections used when importing merchandise into the U.S. These collections were reviewed as candidates for the Customs' "Paperless Entry Project". Based on our review, this collection has been designated for a 1991 time track for incorporation into the Customs' system. Development plans and a timetable for making progres toward the paperless system should be submitted to OMB by August 31, 1989. CDC should notify OMB as early as possible about any problems it encounters during the planning and development process.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/1991	07/31/1991	03/31/1990
Responses	383	0	383
Time Burden (Hours)	111	0	111
Cost Burden (Dollars)	0	0	0

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Abstract: THIS DATA COLLECTION IS THE APPLICATION FOR A PERMIT TO IMPORT OR TRANSFER AGENTS OR VECTORS OF HUMAN DISEASES. THE IMPORTER PROVIDES INFORMATION ON METHODS OF TRANSPORTATION AND PROPOSED USES OF MATERIAL IMPORTED. IN THE INTERSTATE SHIPMENT OF THESE VECTORS, CARRIERS MUST REPORT THE DISCOVERY OF DAMAGED PACKAGES AND THE SENDER MUST REPORT AN LOST SHIPMENTS.

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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

table that charts list of burden

IC Title	Form No.	Form Name
IMPORTATION AND SHIPMENT OF ETIOLOGIC AGENTS	CDC 0.753

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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	383	383	0	0	0	0
Annual Time Burden (Hours)	111	111	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:

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Annual Cost to Federal Government: $0

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 [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

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: 03/09/1989

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