Stem Cell Therapeutic Outcomes Database

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 1 Stem Cell Therapeutic Outcomes Database (Post-Trans)	Form	Modified	Available
Form 2 Stem Cell Therapeutic Outcomes Database (Product Form)	Form	Modified	Available
Form 1 Stem Cell Therapeutic Outcomes Database (Pre-TED Form 2400)	Form	Modified	Repair queued
CIBMTR - HIPAA Ltr PHA Letter 2008Mar26.pdf	Supplementary Document	Uploaded 2013-04-25	Available
Stem Cell Therapeutic and Research Reauthorization Act of 2010.pdf	Supplementary Document	Uploaded 2013-04-25	Available
Supporting Statement.docx	Supporting Statement A	Uploaded 2013-06-11	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
180282	Stem Cell Therapeutic Outcomes Database (Post-Trans)	Form	Modified
180281	Stem Cell Therapeutic Outcomes Database (Product Form)	Form	Modified
180280	Stem Cell Therapeutic Outcomes Database (Pre-TED Form 2400)	Form	Modified

ICR Details

OMB Control No: 0915-0310	ICR Reference No: 201306-0915-002
Status: Historical Active	Previous ICR Reference No: 201009-0915-006
Agency/Subagency: HHS/HSA	Agency Tracking No: 19356
Title: Stem Cell Therapeutic Outcomes Database
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 07/26/2013
	Date Received in OIRA: 06/13/2013
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/2016	36 Months From Approved	12/31/2013
Responses	53,400	0	38,500
Time Burden (Hours)	52,260	0	38,700
Cost Burden (Dollars)	0	0	0

---

Abstract: The Stem Cell Therapeutic and Research Act of 2005 provides for the collection and maintenance of human blood stem cells for the treatment of patients and research. HRSA's Healthcare Systems Bureau has established the Stem Cell Therapeutic Outcomes Database. Operation of this database necessitates certain record keeping and reporting requirements in order to perform the functions related to hematopoietic stem cell transplantation under contract to the HHS. The Act requires the Secretary to contract for the establishment and maintenance of information related to patients who have received stem cell therapeutic products and to do so using a standardized, electronic format. Data is collected from transplant centers by the Center for International Blood and Marrow Transplant Research and is used for ongoing analysis of transplant outcomes. HRSA uses the information in order to carry out its statutory responsibilities. Information is needed to monitor the clinical status of transplantation and to provide the Secretary of HHS with an annual report of transplant center-specific survival data. The increase in burden, as reflected in this revised submission request, is due to an increase in the annual number of transplants and increasing survivorship after transplantation.

---

Authorizing Statute(s): US Code: 42 USC 379A Name of Law: Stem Cell Therapeutic Outcomes Database
   PL: Pub.L. 111 - 264 379 Name of Law: The Stem Cell Therapeutic and Research Act of 2005, PL 109-129, as amended by PL 111-264
  

Citations for New Statutory Requirements: None

---

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

---

Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 14805	03/07/2013
30-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 35039	06/11/2013
Did the Agency receive public comments on this ICR? Yes

---

Number of Information Collection (IC) in this ICR: 3

table that charts list of burden

IC Title	Form No.	Form Name
Stem Cell Therapeutic Outcomes Database (Pre-TED Form 2400)	1	PRE-TED Form 2400
Stem Cell Therapeutic Outcomes Database (Product Form)	2, 3, 1	HLA ,   INF ,   IDM
Stem Cell Therapeutic Outcomes Database (Post-Trans)	1	Post-TED

---

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	53,400	38,500	0	0	14,900	0
Annual Time Burden (Hours)	52,260	38,700	0	0	13,560	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: The increase in burden is due to an increase in the annual number of transplants and increasing survivorship after transplantation.

---

Annual Cost to Federal Government: $3,800,000

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]? 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

---

Common Form ICR:  No

---

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: 06/13/2013

---