Recordkeeping requirements under 510.301 and 514.80

Adverse Experience/Events with Approved New Animal Drugs

OMB: 0910-0284

IC ID: 197284

Documents and Forms
Document Name
Document Type
no available documents/forms check other ICs listed under this ICR
Information Collection (IC) Details

View Information Collection (IC)

Recordkeeping requirements under 510.301 and 514.80
 
No Modified
 
Mandatory
 
21 CFR 514.80 21 CFR 510.301

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability

Health Consumer Health and Safety

 

87 0
   
Private Sector Businesses or other for-profits
 
   99 %

  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 124,444 0 0 119,789 0 4,655
Annual IC Time Burden (Hours) 1,742,136 0 0 1,677,019 0 65,117
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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.

© 2024 OMB.report | Privacy Policy