Information Collection

Subpart D - FDA Action on Applications

IC 184601 under ICR 202507-0910-009 · OMB 0910-0001.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0001 can be found here:

Documents and Forms

Document Name Document Type
0429 GFI PDUFA Meetings.pdf Other-Agency Guidance
0429 GFI PDUFA Meetings.pdf Other-Agency Guidance
CDER CBER Dispute Res at Div Level GFI.pdf Other-Agency Guidance
CDER CBER Dispute Res at Div Level GFI.pdf Other-Agency Guidance

Information Collection (IC) Details

View Information Collection (IC)

IC Title:	Subpart D - FDA Action on Applications	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Unchanged

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 314.100-314.170

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-Agency Guidance			0429 GFI PDUFA Meetings.pdf		Yes	Yes	Fillable Fileable
Other-Agency Guidance			CDER CBER Dispute Res at Div Level GFI.pdf		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 1,693	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 99 %

	Approved	Previously Approved
Annual Number of Responses for this IC	6,279	6,279
Annual IC Time Burden (Hours)	83,584	83,584
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
No associated records found

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

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