Do clinical research plans require more application space than basic research plans?
(Note: assume that clinical protocols, letters of consent, data and safety monitoring plans, survey instruments, etc. would be in application sections outside the Research Plan.) If yes, please explain. • Do you have additional comments about the effects of a shorter application on the NIH application/review process? How to Submit a Response Please submit responses through the following special Web site: http://grants.nih.gov/grants/guide/rfi_files/rfi_research_plan_add.htm (Alternatively, responses may be submitted by sending an email to orosc@csr.nih.gov.) Responses will be accepted until January 5, 2007 All information provided will be processed and analyzed with strict anonymity. The results obtained from the responses to this RFI will be available to the public on the CSR website. http://cms.csr.nih.gov/ Inquiry Inquiries concerning this Notice may be directed to: Cheryl Oros, Ph.D. Director, Office of Planning, Evaluation & Analysis 6701 Rockledge Drive Room 3030, MSC, 7776 Bethe
