FDA CTP Industry Public Meeting Study

Generic Clearance for the Collection of Qualitative Feedback on Food and Drug Administration Service Delivery

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0697 can be found here:

Documents and Forms

Document Name Document Type
App_A_IPMStudy_INVITATION_EMAIL.docx Instruction
App_B_IPMStudy_INSTRUMENT.docx Other-Survey
App_C_IPMStudy_INFORMED_CONSENT.docx Other-InformedConsent
Memo_0910-0697 FDA CTP Industry Public Meeting (IPM) Study.doc Generic Memo IC Document
App_D_18-058CTP - Exempt Approval Notice.pdf Exempt Approval Notice IC Document

Information Collection (IC) Details

IC Title:	FDA CTP Industry Public Meeting Study	Agency IC Tracking Number:	CTP

IC Status: New

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

Document Type	Instrument File	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Instruction	App_A_IPMStudy_INVITATION_EMAIL.docx	Yes	Yes	Fillable Printable
Other-Survey	App_B_IPMStudy_INSTRUMENT.docx	Yes	Yes	Fillable Fileable Signable
Other-InformedConsent	App_C_IPMStudy_INFORMED_CONSENT.docx	Yes	Yes	Fillable Printable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 300	Number of Respondents for Small Entity: 0

Affected Public: Individuals or Households

Percentage of Respondents Reporting Electronically: 0 %

	Approved	Program Change Due to Agency Discretion
Annual Number of Responses for this IC	300	300
Annual IC Time Burden (Hours)	25	25
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
Generic Memo	Memo_0910-0697 FDA CTP Industry Public Meeting (IPM) Study.doc	11/20/2018
Exempt Approval Notice	App_D_18-058CTP - Exempt Approval Notice.pdf	11/20/2018

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