Information Collection

Focus Groups to Investigate Specific Terminology in Prescription Drug Promotion

IC 209154 under ICR 201008-0910-002 · OMB 0910-0677.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0677 can be found here:

Documents and Forms

Documents and forms in this information collection
Document Name	Document Type
CDER INFORMED CONSENT 10-30-13.docx	Other-Informed Consent
CDER RESPONDENT SCREENER 10-30-13.doc	Other-Respondent Screener
FDA CDER MODERATORS GUIDE - DTC ADS 10-30-13.doc	Other-Moderators Guide
OMB Clearance Memo - FDA CDER 10-30-13.doc OMB Clearance Memo - FDA CDER 10-30-13	IC Document

IC Title:

Focus Groups to Investigate Specific Terminology in Prescription Drug Promotion

Agency IC Tracking Number:

IC Status: New

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

table that charts list of instruments
Document Type	Instrument File	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-Informed Consent	CDER INFORMED CONSENT 10-30-13.docx	No	No	Printable Only
Other-Respondent Screener	CDER RESPONDENT SCREENER 10-30-13.doc	No	No	Printable Only
Other-Moderators Guide	FDA CDER MODERATORS GUIDE - DTC ADS 10-30-13.doc	No	No	Printable Only

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records

Title:

FR Citation:

Number of Respondents: 162

Number of Respondents for Small Entity: 0

Affected Public: Individuals or Households

Percentage of Respondents Reporting Electronically: 0 %

table that charts list of burden
	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	162	0	0	0	0	0
Annual IC Time Burden (Hours)	284	0	0	0	0	0
Annual IC Cost Burden (Dollars)	0	0	0	0	0	0

Documents for IC

table that charts IC Documents
Title	Document	Date Uploaded
OMB Clearance Memo - FDA CDER 10-30-13	OMB Clearance Memo - FDA CDER 10-30-13.doc	10/30/2013

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