End Stage Renal Disease Medical Information System, ESRD Facility Survey

Forms and Documents

Document Name	Status

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

IC Document Collections

IC ID	Document Title	Status
8058	End Stage Renal Disease Medical Information System, ESRD Facility Survey Form	Migrated

ICR Details

OMB Control No: 0938-0447	ICR Reference No: 199606-0938-005
Status: Historical Active	Previous ICR Reference No: 199303-0938-008
Agency/Subagency: HHS/CMS	Agency Tracking No:
Title: End Stage Renal Disease Medical Information System, ESRD Facility Survey
Type of Information Collection: Reinstatement with change of a previously approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 08/23/1996
	Date Received in OIRA: 06/20/1996
Terms of Clearance: OMB approves this information collection through August 1997 cont ingent upon compliance with the following conditions: 1.) HCFA removes items 4A-5A, 4B-5B, 14-25, and 30-33. HCFA wil l henceforth collect this information by aggregating patient-spec ific data off of HCFA-2728. This information is collected at th e patient-specific level and can be aggregated on that basis. Th e collection of patient-specfic data and aggregate data on separa te forms is unnecessarily duplicative; and 2.) HCFA will evaluate the practical utility of the data being collected on this form to ensure that all data elements being collected are consistent with HCFA's proposed ESRD Conditions for Coverage of End Stage Renal Disease Facilities regulation and its new core data set

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/1997	08/31/1997
Responses	3,200	0	0
Time Burden (Hours)	25,600	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: The ESRD Facility Survey form (HCFA-2744) is completed annually by Medicare-approved providers of dialysis and transplant services. The HCFA-2744 is designed to collect information concerning treatment trends, utilization of services, and patterns of practice in treating ESRD patients.

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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

IC Title	Form No.	Form Name
End Stage Renal Disease Medical Information System, ESRD Facility Survey	HCFA-2744

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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	3,200	0	0	3,200	0	0
Annual Time Burden (Hours)	25,600	0	0	25,600	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

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: 06/20/1996

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