The iRIS system will receive database updates tonight between 8:30pm and 11pm.

The system will be available during this time, but users should avoid working in the system during this time to avoid losing work.

In August 2019, the UCSF IRB started transferring responsibility for request and maintenance of affiliate access to UCSF networks and applications back to the PI’s department.

This is a follow up to the HRPP Bulletin sent on September 29, 2020. 

In February 2021, UC Office of the President (UCOP) announced new guidance regarding surrogate certification processes.

Background: What Is a Surrogate?

Information Session on Availability of the FDA-compliant (“Part 11 compliant”) version of DocuSign: Tuesday March 23rd

What is happening?

The Human Research Protection Program (HRPP) has updated the May 8, 2020 memo detailing IRB reporting requirements for protocol deviations made in response to COVID-19 and for adherence to the Office of Research Guidance for Onsite Clinical Research Activities.

Per the official UCOP holiday and winter

New! Information Sheet and Consent Form Addendums for COVID-19 Screening and Testing Procedures

The HRPP has created the following documents for research participants attending onsite study visits during the COVID-19 public health emergency:

IRB Limited Meeting Schedule: Impact on Studies Expiring in November, December, January