GFI: Medical Product Communications That Are Consistent with the FDA-Required Labeling – Questions and Answers

Medical Product Communications That Are Consistent With the Food and Drug Administration Required Labeling -Questions and Answers

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0856 can be found here:

Documents and Forms

Document Name Document Type

no available documents/forms check other ICs listed under this ICR

Information Collection (IC) Details

IC Title:	GFI: Medical Product Communications That Are Consistent with the FDA-Required Labeling – Questions and Answers	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Unchanged

Obligation to Respond: Voluntary

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: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 324	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	Previously Approved
Annual Number of Responses for this IC	9,720	9,720
Annual IC Time Burden (Hours)	38,880	38,880
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

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