View Information Collection (IC)

View Information Collection (IC)

Mandatory Adverse Event Reporting via the SRP
 
No Modified
 
Mandatory
 

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Other-Screen shots for CVM collection 0645 IC2 CVM adverse drug experiences and product defects RQ screenshots 2013.pdf Yes No Paper Only

Health Consumer Health and Safety

 

636 0
   
Individuals or Households
 
   100 %

  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 636 0 0 -127,767 0 128,403
Annual IC Time Burden (Hours) 636 0 0 -127,767 0 128,403
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.