Information Collection

CDER Export Certificate (FDA 3613f)

IC 217014 under ICR 202303-0910-018 · OMB 0910-0498.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0498 can be found here:

Documents and Forms

Documents and forms in this information collection
Document Name	Document Type
CDER eCATS API Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS API Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS- Approved Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS- Approved Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS- OTC Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS- OTC Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS -Unapproved Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
CDER eCATS -Unapproved Drug FlowFINAL03072016.pdf	Other-Screenshots of electronic subm
FDA 3613f REQUEST FOR CERTIFICATE OF A PHARMACEUTICAL PRODUCT FOR Form FDA 3613f CDER.pdf	Form and Instruction
FDA 3613f REQUEST FOR CERTIFICATE OF A PHARMACEUTICAL PRODUCT FOR Form FDA 3613f CDER.pdf	Form and Instruction

IC Title:

CDER Export Certificate (FDA 3613f)

Agency IC Tracking Number:

Is this a Common Form? No

IC Status: Unchanged

Obligation to Respond: Required to Obtain or Retain Benefits

CFR Citation: 21 CFR 1.101

Information Collection Instruments:

table that charts list of instruments
Document Type	Form No.	Form Name	Instrument File	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-Screenshots of electronic submission of API Drug			CDER eCATS API Drug FlowFINAL03072016.pdf	Yes	Yes	Fillable Fileable
Other-Screenshots of electronic submission of Approved Drug			CDER eCATS- Approved Drug FlowFINAL03072016.pdf	Yes	Yes	Fillable Fileable
Other-Screenshots of electronic submission for CDER OTC Drug			CDER eCATS- OTC Drug FlowFINAL03072016.pdf	Yes	Yes	Fillable Fileable
Other-Screenshots of electronic submission of Unapproved Drug			CDER eCATS -Unapproved Drug FlowFINAL03072016.pdf	Yes	Yes	Fillable Fileable
Form and Instruction	FDA 3613f	REQUEST FOR CERTIFICATE OF A PHARMACEUTICAL PRODUCT FOR CDER PRODUCTS	Form FDA 3613f CDER.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: 3,680

Number of Respondents for Small Entity: 0

Affected Public: Private Sector

Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 0 %

table that charts list of burden
	Approved	Previously Approved
Annual Number of Responses for this IC	3,680	3,680
Annual IC Time Burden (Hours)	3,680	3,680
Annual IC Cost Burden (Dollars)	644,000	644,000

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.