Information Collection

Adverse Experience Reporting for Licensed Biological Products and General Records -- 21 CFR 600

IC 5874 under ICR 199903-0910-001 · OMB 0910-0308.

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Information Collection (IC) Details

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IC Title:	Adverse Experience Reporting for Licensed Biological Products and General Records -- 21 CFR 600	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: 391	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
Annual Number of Responses for this IC	3,212	3,212
Annual IC Time Burden (Hours)	342,132	342,132
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

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