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Studies to Enhance FDA Communications Addressing Biosimilar Drug Products: Focus Groups and INterviews with Healthcare Professionals CDER
 
New
 
Voluntary
 

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Other-Survey Instrument Yes No Paper Only
Other-Consent form - focus groups Yes No Paper Only
Other-Consent form - individual groups Yes No Paper Only
Other-Invitation Email Yes No Paper Only
Other-Appointment confirmation email Yes No Paper Only
Other-Interview guide No   Paper Only
Other-Moderator guide No   Paper Only

Health Consumer Health and Safety

 

316 0
   
Individuals or Households
 
   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 316 0 316 0 0 0
Annual IC Time Burden (Hours) 263 0 263 0 0 0
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
OMB approval memo 04/16/2018
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.
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