Reporting: Annual drug experience report Form FDA 2301

Records and Reports Concerning Experience with Approved New Animal Drugs

OMB: 0910-0284

IC ID: 197280

Documents and Forms
Document Name
Document Type
Form and Instruction
Other-Screenshots - Proposed Electro
Form and Instruction
Information Collection (IC) Details

View Information Collection (IC)

Reporting: Annual drug experience report Form FDA 2301 CVM
 
No Modified
 
Mandatory
 
21 CFR 514.80(b)(4)

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Form and Instruction 2301 Transmittal of Periodic Reports and Promotional Material Form FDA 2301.pdf No No Paper Only
Other-Screenshots - Proposed Electronic Submitter System 0284 Screenshots.doc Yes Yes Fillable Fileable

Health Consumer Health and Safety

 

200 0
   
Private Sector Businesses or other for-profits
 
   0 %

  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 1,622 0 0 0 0 1,622
Annual IC Time Burden (Hours) 25,952 0 0 0 0 25,952
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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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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