One Health Harmful Algal Bloom System (OHHABS)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Att. H - List of OHHABS reporting sites.pdf	Supplementary Document	Uploaded 2019-01-17	Available
Att. G - PIA.pdf	Supplementary Document	Uploaded 2019-01-17	Available
Att. F - OHHABS Reporting Workflow.docx	Supplementary Document	Uploaded 2019-01-17	Available
Att. E - HAB Case and Event Definitions Table.pdf	Supplementary Document	Uploaded 2019-01-17	Available
Att. D - Non-research determination.pdf	Supplementary Document	Uploaded 2019-01-17	Available
Att. B - 60-day FRN.pdf	Supplementary Document	Uploaded 2019-01-17	Available
SS_B_0920-1105_One Health Harmful Algal Bloom System (OHHABS) 28Dec2018.....docx	Supporting Statement B	Uploaded 2019-01-17	Repair queued
SS_A_0920-1105_One Health Harmful Algal Bloom System (OHHABS) 28Dec2018 ....doc	Supporting Statement A	Uploaded 2019-01-17	Available
Att A_Authorizing_Regulations_T42_section_241.doc	Supplementary Document	Uploaded 2015-09-17	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
218236	Harmful Algal Bloom-related Illness Surveillance System	Other-Data elements	Modified

ICR Details

OMB Control No: 0920-1105	ICR Reference No: 201901-0920-004
Status: Active	Previous ICR Reference No: 201701-0920-009
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-1105
Title: One Health Harmful Algal Bloom System (OHHABS)
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: 03/21/2019
	Date Received in OIRA: 02/08/2019
Terms of Clearance: Previous terms continue: OMB is approving this information collection request for a period of three years. Any communications or publications that arise from this collection will include a clear description of the reporting entities (e.g., which states/territories voluntarily participate) and a discussion of how their reporting and monitoring practices may differ. As it is anticipated that HAB-related case definitions, data collection instruments, and protocols will evolve over time through the analysis of data gathered in OHHABS, the agency will submit such changes to OMB via an ICR Revision request. If such updates are within the confines of the general concepts and approaches approved within this OMB clearance (i.e., refinements rather than new concepts) CDC may use a non-substantive change request to submit such changes.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	03/31/2022	36 Months From Approved	03/31/2019
Responses	171	0	171
Time Burden (Hours)	57	0	57
Cost Burden (Dollars)	0	0	0

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Abstract: The goal of the One Health Harmful Algal Bloom System (OHHABS) is to collect data on harmful algal blooms (HABs) and human and animal illnesses related to HAB exposures. Data collected in OHHABS will be accessible to state health departments, federal partners and other stakeholders to better characterize HAB events and single human and animal illness related to HAB exposures and to inform future prevention efforts.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: PHSA
  

Citations for New Statutory Requirements: None

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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:
	83 FR 51958	10/15/2018
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 2513	02/07/2019
Did the Agency receive public comments on this ICR? Yes

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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
Harmful Algal Bloom-related Illness Surveillance System

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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	171	171	0	0	0	0
Annual Time Burden (Hours)	57	57	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: $145,000

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

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

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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: 02/08/2019

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