Registration for the Clinical Trials Reporting Program (CTRP) Database (NCI)

The Clinical Trials Reporting Program (CTRP) Database (NCI)

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0925-0600 can be found here:

Documents and Forms

Document Name Document Type
Form 1 Registration for the Clinical Trials Reporting Program (CTRP) Database (NCI) Form
1 CTRP Registration Attachment_2A_FORM_CTRP Registration.doc Form
Attachment_3_INSTRUCT_CTRP Registration_Site_Users_Guide.pdf Registration Site Users Guide IC Document

Information Collection (IC) Details

IC Title:	Registration for the Clinical Trials Reporting Program (CTRP) Database (NCI)	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Modified

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form	1	CTRP Registration	Attachment_2A_FORM_CTRP Registration.doc		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Public Health Monitoring

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 5,500	Number of Respondents for Small Entity: 500

Affected Public: Individuals or Households

Percentage of Respondents Reporting Electronically: 100 %

	Approved	Previously Approved
Annual Number of Responses for this IC	5,500	5,500
Annual IC Time Burden (Hours)	11,000	11,000
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
Registration Site Users Guide	Attachment_3_INSTRUCT_CTRP Registration_Site_Users_Guide.pdf	01/15/2010

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