The webinar will address concerns raised and actions taken to date by federal intelligence and research funding agencies.

This webinar will examine the different types of ancillary research agreements, when and why they are necessary, and highlight potential negotiation areas.

This webinar will explore the federal requirements surrounding cost transfers and examine how two different institutions have implemented policies to monitor compliance and mitigate the risk associated with these types of transactions.

Assessing and identifying organizational training needs from the outset is important for designing and preparing educational materials to achieve the desired learning outcomes.

This webinar will provide an overview of the impact of the Common Rule (45 CFR part 46) changes on HIPAA (Health Insurance Portability and Accountability Act) (45 CFR Part 160 and Part 164) covered information and biospecimens.

This webinar will provide a description of the function of Offices of Inspectors General (OIGs), the OIG’s that impact the research community, and 2019 OIG audit plans.

In this webinar, we will explore everything that a Departmental Administrator needs to know in working with federal contracts for sponsored projects.

This session will focus on how to evaluate GDPR risk and building sustainable privacy programs using real world examples from higher education.

This workshop will examine a variety of regulations that impact the day-to-day management of federal awards with the goal of helping participants answer these questions, and to better understand where regulations end and institutional policies begin.

This workshop provides a primary basis of understanding of proposals to and awards from the National Institutes of Health (NIH).

This workshop is a professional development opportunity that focuses primarily on the financial regulatory compliance aspects of Research Administration.