Information Collection

Subpart D - FDA Action on Applications

IC 184601 under ICR 202402-0910-003 · 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⚠️ Notice: This information collection may be referencing outdated material.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

Documents and forms in this information collection
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

IC Title:

Subpart D - FDA Action on Applications

Agency IC Tracking Number:

Is this a Common Form? No

IC Status: Modified

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 314.100-314.170

Information Collection Instruments:

table that charts list of 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 %

table that charts list of burden
	Approved	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	6,279	-387	6,666
Annual IC Time Burden (Hours)	83,584	-194	83,778
Annual IC Cost Burden (Dollars)	0	0	0

Documents for IC

table that charts IC Documents
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.