Frequently asked questions (FAQs) related to RFP-IV have been cataloged here. You may view existing FAQs by using the tabs on this page to filter by recently asked questions (Q&A tab) or by category (Categories tab). To see all existing questions for RFP-IV use the Print FAQ tab. You can also use the above search field to find questions and answers by entering a keyword related to your inquiry. If you do not find an answer to your question after reviewing the FAQs, you may submit a new question by clicking on the Submit a Question tab.

Does GoMRI adhere to federal law requirements for subject research protection and confidentiality? What human subject use requirements, including data requirements, will GoMRI implement?

131 views asked in Awards and Contracting by mlichtve
edited by faqeditor

1 Answer

Yes, GoMRI follows the National Science Foundation's policy (and federal law) regarding human subject use (http://www.nsf.gov/bfa/dias/policy/human.jsp). GRIIDC will not handle and archive human subject research data or data requiring Institutional Review Board (IRB) certification. All data requiring such certification will remain in the possession of and be managed by the IRB-certified researcher. However, these data will be recorded in the Data Source Registry (DSR). For more information about GRIIDC data policies, please see the GRIIDC Data Management Plan, posted under "Design and Management," on the GoMRI Data Management Web site (https://data.gulfresearchinitiative.org/).
answered by faqeditor
Powered by Question2Answer

Web design by Will Ramos | © Copyright Gulf Research Initiative (GoMRI) 2013-2014. All Rights Reserved.

...