Adverse Experience Reporting for Licensed Biological Product; and General Records

Adverse Experience Reporting for Licensed Biological Product; and General Records

OMB: 0910-0308

IC ID: 5877

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)

Adverse Experience Reporting for Licensed Biological Product; and General Records
 
No Migrated
 
Mandatory
 

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


    

320 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 22,324 0 0 -2,396 0 24,720
Annual IC Time Burden (Hours) 493,522 0 0 -83,071 0 576,593
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
 
 
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.

© 2024 OMB.report | Privacy Policy