Recent Policy Updates

Clarified responsibility of the individual researcher.

Clarified in regard to the medical oversight of the program.

Provides comprehensive information about the organization, scope, authority and responsibilities associated with Stanford University's program for the protection of human research subjects.

Provision for publication delays in the case of multi-site clinical research projects.

Definition of research misconduct revised and other clarifications incorporated.

Presents principles, guidelines and procedures for the establishment and operation of membership-sponsored programs designed to facilitate a productive relationship between Stanford and industry. Additional program requirements established in January 2006 by memo from the Vice Provost and Dean of Research. 

Closeout requirements were added.

Discusses the responsibilities for use of human subjects in student projects, pilot studies and oral histories (non-medical), and describes conditions under which Administrative Panel review and approval is needed.

Presents an explanation of Stanford University's Facilities & Administrative (Indirect Cost) and Fringe Benefits Rates, including definitions of "on-campus" and "off-campus" rates, and Modified Total Direct Costs (MTDC). Current rates are maintained by the Cost & Management Analysis Office. 

Establishes principles and procedures designed to ensure that research involving human subjects at Stanford University is conducted without untoward influence resulting from either the University's financial investments or holdings or the personal financial interests or holdings of key institutional leaders.