Information Collection

Good Manufacturing Practices For Blood And Blood Components - 21 Cfr Part 606

IC 109621 under ICR 198408-0910-009 · OMB 0910-0116.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0116 can be found here:

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Information Collection (IC) Details

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IC Title:	GOOD MANUFACTURING PRACTICES FOR BLOOD AND BLOOD COMPONENTS - 21 CFR PART 606	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Migrated

Obligation to Respond: Mandatory

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability

Line of Business:

Subfunction:

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 40	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 0 %

	Approved	Program Change Due to Agency Discretion	Previously Approved
Annual Number of Responses for this IC	2,060	0	2,060
Annual IC Time Burden (Hours)	3,000,000	-40	3,000,040
Annual IC Cost Burden (Dollars)	0	0	0

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Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.