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Clinical Trials Reporting Program
Posted:
04/24/2009
Clinical Trials Reporting Program
About CTRP
Who Registers, What Trials & When
How to Register Trials
Frequently Asked Questions (FAQs)
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Frequently Asked Questions - FAQs
CTRP Program
>>
What is the purpose of the Clinical Trials Reporting Program (CTRP)?
How will CTRP be connected to other databases within NCI and NIH?
Will CTRP support the Cancer Centers Summary 4 Report?
Will CTRP register my trials with clinicaltrials.gov for me?
If I register a trial with CTRP, will CTRP send the trial to PDQ?
Expectations for Grantees
>>
How do I register trials with CTRP?
What trials does NCI expect to be registered in CTRP?
What data do I need to report and when?
Registration
>>
Are usernames and passwords required to register trials to CTRP?
Is batch registration available?
Will NCI work with us and/or our vendor to develop a link to CTRP?
How do I know that my trials have been registered successfully?
When can I view a trial?
How do I modify trials or handle errors?
How do I know if a trial has been previously submitted to NCI?
What formats are acceptable for uploaded supporting trial documents?
What is the NCI Division/Program Code?
What should be in the NCI Grant Information section?
CTRP Orientation, Communications, and Support
>>
How does NCI intend to notify grantees about CTRP reporting?
Is there a mailing list to receive CTRP communications?
What type of training or orientation will be provided?
How do I get support and find further information?
Whom can I contact for assistance?
Data Access
>>
Will I have access to data from my submissions?
Will it be shared with grantees or others outside of NCI?
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