We want to remind the research community about relevant NIH inclusion policies and resources, as well as where inclusion data can be found. Appropriate inclusion of research participants ensures that NIH supports science that will inform clinical practice to benefit all who are affected by the disease or condition under study.
Domestic institutions with an approved Domestic Animal Welfare Assurance are reminded that Annual Reports for the reporting period October 1, 2022, through September 30, 2023, are due to the NIH Office of Laboratory Animal Welfare (OLAW) by December 1, 2023. (NOT-OD-24-008). These reports cover the October 1, 2022, through September 30, 2023 reporting period.
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In this episode of the NIH All About Grants podcast, Deysi Duque, a Senior Clinical Trials Analyst within the NIH Office of Extramural Research, talks us through the clinical trials dissemination policy, its purpose, resources, exceptions, and what recipient organizations and researchers should know to ensure compliance.
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The Human Subjects and Clinical Trials Information form appears for all recipients with human subjects studies. However, those who submitted competing applications for due dates on or before January 25, 2018 only need to update inclusion data via the Human Subjects link in the RPPR. The remaining fields (e.g. milestones) are not required to be … Continue reading “In the RPPR, do we need to fill out the Human Subjects and Clinical Trials Information form if we submitted a competing application before January 25, 2018?”
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In the Final RPPR you should report on the individuals that worked on the project during the last budget period minus any approved no-cost extensions. You can find this and more in the RPPR FAQs.
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