Public Health Service Policies on Research Misconduct (42 CFR Part 93)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 6349 Public Health Service Policies on Research Misconduct (42 CFR Part 93)	Form	Modified	Available
ORI_MEMORANDUM_OMB_REQUEST.pdf	Justification for No Material/Nonsubstantive Change	Uploaded 2013-11-21	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
7747	Public Health Service Policies on Research Misconduct (42 CFR Part 93)	Form	Modified

ICR Details

OMB Control No: 0937-0198	ICR Reference No: 201311-0937-001
Status: Historical Inactive	Previous ICR Reference No: 201205-0937-001
Agency/Subagency: HHS/OASH	Agency Tracking No: 20983
Title: Public Health Service Policies on Research Misconduct (42 CFR Part 93)
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Improperly submitted and continue	Conclusion Date: 11/22/2013
	Date Received in OIRA: 11/21/2013
Terms of Clearance: Burden associated with the form 6315 was not disscussed in the previous request and the burden has not been accounted for in the current request. If no prior approval of the form was granted, a revision request must be submitted following the required notice and comment periods.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	06/30/2015	06/30/2015	06/30/2015
Responses	6,096	0	6,096
Time Burden (Hours)	1,016	0	1,016
Cost Burden (Dollars)	0	0	0

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Abstract: Section 493 of the Public Health Service Act and 42 CFR Part 93 requires each institution that applies for research and research- related grants to estabish policies and procedures for investigating and reporting instances of alleged or apparent research miscondut for activity supported by PHS funds and to report such instances to the Secretary.

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Authorizing Statute(s): PL: Pub.L. 99 - 158 493 Name of Law: Health Research Extension Act of 1985
  

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
Public Health Service Policies on Research Misconduct (42 CFR Part 93)	6349, 6315	PHS ,   PHS

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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: $38,685

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

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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: 11/21/2013

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