View Information Collection (IC)
View Information Collection (IC)

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Focus Group Testing of Consumer Messaging on Participation of Diverse Women in Clinical Trials OC
 
New
 
Voluntary
 

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Other-Moderator Guide Clinical Trials Moderator Guide FINAL 07_02_15.doc No   Printable Only
Other-Screener Guide Clinical Trials Screener Guide FINAL 07_01_15.doc No   Printable Only
Other-Consent Form Consent Form_Clinical Trials_FINAL 07_01_15.docx No   Printable Only
Other-Fact Sheet Check Fact Sheet Check_Clinical Trials FINAL 07_02_15.docx No   Printable Only
Other-Flyer WomenandClinicalTrials_Flyer_Draft copy.docx No   Printable Only
Other-Clinical Trials Information Sheet Clinical Trials 2013.pdf No   Printable Only

Health Consumer Health and Safety

 

99 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 99 0 99 0 0 0
Annual IC Time Burden (Hours) 42 0 42 0 0 0
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
Supporting Statement Memo FDA OWH Diverse Women in Clinical Trials Focus Groups - OMB 0910-0497.doc 07/30/2015
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.