Institutional Review Board (IRB)
The government has strict guidelines and safeguards in place to protect people who volunteer to participate in a clinical trial. In the United States, each clinical trial must be approved and monitored by an Institutional Review Board (IRB) to ensure the risks to the study participants are as low as possible. At Dignity Health all human subjects research activity must be reviewed by a Dignity Health internal IRB or an external IRB approved by Dignity Health.
Training & Education
DHRI has dedicated personnel to ensure that all research staff have access to the proper resources and are up to date on the most recent regulations and policies. For any training related questions, requests, or concerns please reach out to the Training & Education team at (916) 851-2685.
Dignity Health utilizes the Collaborative Institutional Training Initiative (CITI) Program for basic human subjects research training required for all clinical research investigators at Dignity Health. To access CITI please click here. To learn more about Dignity Health Research Institute basic training and education requirements, please click on the link below. This link is intended for Dignity Health associates and employees only. If you need help accessing this resource please contact the Training & Education team at (916) 851-2283 or email us at [email protected] with the subject line ATTN Training.
Policies & Procedures
Dignity Health Research Institute Policies and Procedures assure that all research conducted at a Dignity Health facility adheres to all applicable laws, regulations and ethical guidelines.
For a complete list of Dignity Health Research Institute Policies, or to contact the Policy Manager administrator click on the button below. This page is intended for Dignity Health associates and employees only.If you need help accessing this resource please contact the Training & Education team at (916) 851-2285 or email us at [email protected] or in the questions form below with the subject line ATTN Training.