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When
your proposal is funded by NHLBI, you agree to be bound by
the terms and conditions outlined in the Notice of Grant
Award. They take effect as soon as grant funds are drawn
down. It's important that you pay careful attention
to the terms and conditions of your award before you begin
the project period as changes may have occurred from what
you had initially proposed. These changes can occur
in your budget, specific aims or in the duration of your
award.
In some instances we might place a restriction on your award,
restricting it from a particular activity, such as human
subjects testing, until paperwork is received and processed. This
section will help you to define which activities must be
completed before you can begin your clinical study and will
answer these questions:
- How do I know if I am funded?
- Who needs human subjects protection training?
- Who approves my data monitoring plan?
- What is a Certificate of Confidentiality and do I need one?
- How do I develop consent forms and who reviews them?
- Do I need IRB, IEC or REB approval?
- Are there ethical concerns and conflicts of interest
I must consider?
- What other approvals are needed?
- How do I track recruitment
of research participants?
- My study involves
Medicare or third party support.
- My study involves
foreign grants and contracts.
- How do I register my study?
- When can I begin enrolling
participants?
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