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View ICR - OIRA Conclusion

OMB Control No: 0910-0582	ICR Reference No: 200601-0910-001
Status: Historical Active	Previous ICR Reference No:
Agency/Subagency: HHS/FDA	Agency Tracking No:
Title: Guidance on Informed Consent for in Vitro Diagnostic Studies Using Leftover Human Specimens that are not Individually Identifiable
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: 01/24/2006
OIRA Conclusion Action: Approved with change	Conclusion Date: 03/13/2006
	Date Received in OIRA: 01/06/2006
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2006	09/30/2006
Responses	600	0	0
Time Burden (Hours)	2,400	0	0
Cost Burden (Dollars)	0	0	0

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