Know Which Types of Items are Controlled

“Dual-Use” Technologies The controlled technologies most commonly found on campus are “dual-use” technologies covered by the Export Administration Regulations (EAR). These are items or technologies with potential for both civilian and military use (the military use may not be obvious). Dual-use items can be found on the Commerce Control List (CCL). Each category on the CCL […]

Determine Agency Jurisdictions Over Exports

Two primary sets of regulations govern the export of controlled technologies: the International Traffic in Arms Regulations (ITAR)​ and the Export Administration Regulations (EAR). The ITAR, which are administered and enforced by Department of State through its Directorate of Defense Trade Controls (DDTC), regulate the export of military, space, and satellite technologies. The EAR, which are administered and enforced […]

Define “U.S. Person” vs. “Foreign National”

A “U.S. Person” is defined as a: ​Lawful Permanent Resident U.S. Citizen Legal Immigrant with a “Green Card” Protected Individual granted asylum or refugee status “Foreign National” includes everyone else, including foreign governments or entities not incorporated to do business in the U.S.

Determine When Export Control Laws Apply

What is export control? Export control laws regulate the export of commodities, related technical data and information, and certain services the federal government considers critical to the national security or domestic economy of the United States. The export control laws also regulate the transfer of controlled technical data to foreign nationals within the United States (“deemed exports”). “Exports” are […]

Determine if Your Trial Needs to Be Registered on Clinicaltrials.gov

Which trials are required to be registered by law? The law states that an applicable clinical trial generally includes (1) Trials of Drugs and Biologics: Controlled, clinical investigations, other than Phase I investigations, of a product subject to FDA regulation and (2) Trials of Devices: Controlled trials with health outcomes, other than small feasibility studies, […]

Guide to Developing a NIH RCR Plan

For Institutional Training and Career Development Programs such as T32, T34, T90/R90, TL1, K12, K30 Purpose This RCR Plan Worksheet is meant as a guide to help Washington University investigators develop appropriate RCR education plans in compliance with current NIH requirements. Individual Principal Investigators are responsible for developing, implementing, monitoring, and reporting on his/her RCR education plans. WashU […]

Develop RCR Programming

There are many resources available to help in developing RCR educational programming. Below are internal resources and resources recommended by funding agency. For general resources, visit Resources on the Web. National Institutes of Health (NIH) Beginning January 25, 2010, the NIH requires RCR education plans to be submitted with all new and renewal applications for NIH-funded programs supporting […]