Information Collection

Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802

IC 188598 under ICR 200903-0910-006 · OMB 0910-0498.

Documents and Forms

Documents and forms in this information collection
Document NameDocument Type
Form FDA 3613a
Supplementary Information Certificate of Exportability Requests Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Form and Instruction
Form FDA 3613
Supplementary Information Certificate to Foreign Government Requests Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Form and Instruction
Form FDA 3613b
Supplementary Information Certificate of a Pharmaceutical Product Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Form and Instruction
Form FDA 3613c
Supplementary Information Non-Clinical Research Use Only Certificate Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Form and Instruction
Form FDA 3613d
Office of Cosmetics and Colors "Certificate" Export Application Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Form and Instruction
Form FDA 3613e
Food Export Certificate Application Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Form and Instruction
FDA 3613a Supplementary Information Certificate of Exportability R
FDA-3613a.pdf
Form and Instruction
FDA 3613 Supplementary Information Certificate to Foreign Governm
FDA-3613.pdf
Form and Instruction
FDA 3613b Supplementary Information Certificate of a Pharmaceutica
FDA-3613b.pdf
Form and Instruction
FDA 3613c Supplementary Information Non-Clinical Research Use Only
FDA-3613c.pdf
Form and Instruction
FDA 3613d Office of Cosmetics and Colors "Certificate" Export Appl
FDA-3613d.pdf
Form and Instruction
FDA 3613e Food Export Certificate Application
FDA-3613e.pdf
Form and Instruction

Information Collection (IC) Details

View Information Collection (IC)

layout table

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
Form and Instruction FDA 3613a Yes No Paper Only
Form and Instruction FDA 3613 Yes No Paper Only
Form and Instruction FDA 3613b Yes No Paper Only
Form and Instruction FDA 3613c Yes No Paper Only
Form and Instruction FDA 3613d Yes No Paper Only
Form and Instruction FDA 3613e Yes No Paper Only

Federal Enterprise Architecture Business Reference Module


table that charts list of burden
  Approved Program Change Due to New Statute Program Change Due to Agency Discretion Change Due to Adjustment in Agency Estimate Change Due to Potential Violation of the PRA Previously Approved
Annual Number of Responses for this IC 8,970 0 0 8,970 0 0
Annual IC Time Burden (Hours) 17,940 0 0 17,940 0 0
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Documents for IC
table that charts IC Documents
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.
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