Archived
Action Items for the Streamlining Working Group
The document outlines the action items of the Streamlining Working Group, aimed at enhancing efficiency and harmonization among foundations and research institutions in key administrative areas. The group plans to form specialized sub-groups focusing on (A) portal and application/proposal systems, (B) financial reporting and invoicing, and (C) common policies and terms such as data sharing and con
Alternatives to Effort Reporting
The document summarizes a presentation delivered at the October 2017 COGR Meeting in Washington, D.C., focused on exploring alternatives to traditional effort reporting in research administration. Initiated by the National Council of University Research Administrators (NCURA) in January 2016, the Cohort project brought together 90 diverse research institutions to develop and promote model policies
HHS and NIH Research Regulatory Reform
The document from the Council on Governmental Relations (COGR) provides a comprehensive analysis of regulatory challenges faced by research institutions under the U.S. Department of Health and Human Services (HHS) and the National Institutes of Health (NIH). It details longstanding concerns about the escalating administrative burden and costs associated with federal research regulations, highlight
Recommendations for HHS and NIH Research Regulatory Reform
The document critically examines the expanding regulatory and administrative burdens faced by U.S. academic research institutions engaged in federally funded research, particularly under the Department of Health and Human Services (HHS) and the National Institutes of Health (NIH). Despite a series of expert and congressional reports since the late 1990s recommending streamlining and harmonization
Discussion Points on Facilities and Administrative Costs and Regulatory Reform
The document discusses the intersection of facilities and administrative (F&A) costs with ongoing efforts to reform research regulations in the United States. It emphasizes that while research institutions and academic medical centers support reducing unnecessary federal regulations to improve the use of research funds, any anticipated reduction in F&A costs tied to decreased regulatory bu
June 2017 Presentation: Key ClinicalTrials.gov Reporting Requirements
The document provides a detailed overview of ClinicalTrials.gov, emphasizing its role as a public registry and results database for clinical studies involving human participants, encompassing interventional trials, observational studies, and expanded access programs across more than 200 countries. Managed by the National Institutes of Health (NIH), ClinicalTrials.gov facilitates transparency, acco
F&A Frequently Asked Questions
The document provides an in-depth explanation of Facilities and Administrative (F&A) costs—also known as indirect costs—associated with federally sponsored research at U.S. universities. F&A costs are essential for maintaining the infrastructure and administrative support required to conduct high-quality research, including laboratory facilities, data management, compliance with health and
