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View ICR - OIRA Conclusion

OMB Control No: 0910-0582	ICR Reference No: 201302-0910-004
Status: Historical Active	Previous ICR Reference No: 201001-0910-007
Agency/Subagency: HHS/FDA	Agency Tracking No: 18779
Title: Guidance on Informed Consent for in Vitro Diagnostic Studies Using Leftover Human Specimens that are not Individually Identifiable
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: 04/10/2013
	Date Received in OIRA: 02/11/2013
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	04/30/2016	36 Months From Approved	04/30/2013
Responses	700	0	700
Time Burden (Hours)	2,800	0	2,800
Cost Burden (Dollars)	0	0	0

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