600.81

Adverse Experience Reporting for Licensed Biological Product; and General Records

OMB: 0910-0308

IC ID: 185788

Documents and Forms
Document Name
Document Type
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Information Collection (IC) Details

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600.81
 
No Modified
 
Mandatory
 
21 CFR 600.81

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

Health Consumer Health and Safety

 

108 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 349 0 0 170 0 179
Annual IC Time Burden (Hours) 349 0 0 170 0 179
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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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