Information Collection

Reporting: Alternative Test Method (FDA 3979) and Waiver from Electronic Submission

IC 225135 under ICR 201701-0910-008 · OMB 0910-0830.

Documents and Forms

Document Name Document Type
Form FDA 3979 Reporting: Alternative Test Method (FDA 3979) and Waiver from Electronic Submission Form and Instruction
FDA 3979 Alternative Test Method Notification FDA-3979 Final.pdf Form and Instruction

Information Collection (IC) Details

View Information Collection (IC)

IC Title:	Reporting: Alternative Test Method (FDA 3979) and Waiver from Electronic Submission	Agency IC Tracking Number:	CTP

Is this a Common Form? No		IC Status: New

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 1132

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	FDA 3979	Alternative Test Method Notification	FDA-3979 Final.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: 23	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 99 %

	Requested	Program Change Due to Agency Discretion
Annual Number of Responses for this IC	23	23
Annual IC Time Burden (Hours)	462	462
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.