Data Collection for Ebola Virus Disease Patients Treated Outside of West Africa

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
US-WHO Clinical Network Ebola Virus Disease Clinical Data Collection Tool	Form and Instruction	New	Repair queued
EmerRqustMemo US-WHO ClinNetwrk EVD ClinDataColl 20150108.pdf	Supplementary Document	Uploaded 2015-01-09	Repair queued
AppndxD SORN 09-20-0113 Epidemic Invest Case Records.pdf	Supplementary Document	Uploaded 2015-01-09	Repair queued
AppndxB Email Invitation and Consent 20150109 V3.docx	Supplementary Document	Uploaded 2015-01-09	Repair queued
AppndxA 42 USC 241 PH Service Act Section 301.pdf	Supplementary Document	Uploaded 2015-01-09	Repair queued
SupStmnt B US-WHO ClinNetwork EVD ClinDataColl 20150108.docx	Supporting Statement B	Uploaded 2015-01-09	Repair queued
SupStmnt A US-WHO ClinNetwork EVD ClinDataColl 20150108 V2 clean.docx	Supporting Statement A	Uploaded 2015-01-09	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
214540	US-WHO Clinical Network Ebola Virus Disease Clinical Data Collection Tool	Form and Instruction	New

ICR Details

OMB Control No:	ICR Reference No: 201501-0920-005
Status: Historical Inactive	Previous ICR Reference No:
Agency/Subagency: HHS/CDC	Agency Tracking No: 15KJ
Title: Data Collection for Ebola Virus Disease Patients Treated Outside of West Africa
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Emergency	Approval Requested By: 01/12/2015
OIRA Conclusion Action: Withdrawn	Conclusion Date: 01/09/2015
	Date Received in OIRA: 01/09/2015
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date		6 Months From Approved
Responses	0	0	0
Time Burden (Hours)	0	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: Pursuant to the Office of Management and Budget (OMB) procedures established under 5 CFR 1320, Controlling Paperwork Burdens on the Public, the CDC requests that the following collection of information, "Data Collection for Ebola Virus Disease Patients Treated Outside of West Africa," be processed in accordance with Section 1320.13 Emergency Processing. This information collection is essential to CDC's mission to support the 2014 Ebola Virus Response in West Africa. The CDC cannot reasonably comply with the normal clearance procedures under the Paperwork Reduction Act (PRA) because delays in information collection are likely to result in continued public harm, illness, and possibly death among patients who must be medically evacuated from the affected countries, patients from West Africa who developed symptoms after leaving (imported patients), and patients who had transmission of Ebola virus outside of Africa. CDC seeks to collect this information retrospectively from clinicians who provided medical care for EVD patients. The clinicians and centers caring for these patients are part of a CDC/WHO International Clinical Network on Clinical Management of Ebola Virus Disease Patients that regularly convenes by phone to discuss the real-time management of these patients.

Emergency Justfication: This is an emergency request for 30-day Office of Management and Budget (OMB) Paperwork Reduction Act (PRA) approval to allow the Centers for Disease Control and Prevention (CDC) to collect clinical data on the presentation, course, and management of patients with Ebola virus disease (EVD) cared for in higher-resource settings in Western Europe and the United States (US). This information collection is necessary to inform the public health response to the Ebola outbreak. Due to the urgent need for this information for dissemination to global audiences in a timely manner, the CDC is requesting that OMB approval is granted by January 12, 2015.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: Public Health Services Act
  

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

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
US-WHO Clinical Network Ebola Virus Disease Clinical Data Collection Tool	None	US-WHO INTERNATIONAL CLINICAL NETWORK EBOLA VIRUS DISEASE CLINICAL DATA COLLECTION TOOL

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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: No

Burden Reduction Due to:

Short Statement: The submission 0920-15KJ is a NEW ICR.

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Annual Cost to Federal Government: $1,662

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: 01/09/2015

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