Standard Operating Procedures

Standard Operating Procedures detail the regular work processes that may be conducted during a clinical research project. They are designed to help researchers maintain consistent quality control and quality assurance, support data quality, and ensure compliance with Creighton University policies and governmental regulations.


Conducting a Study

 Roles and Responsibilities

 Informed Consent and Other Documentation

 Clinical Procedures

 IRB and Regulatory Agencies

Confidential Research Hotline (402-280-3200)

Research Personnel are expected to report any known or suspected noncompliant conduct related to research or sponsored program activities conducted and/or approved through Creighton University. The confidential Research Compliance Hotline (402-280-3200) is available for any individual who wishes to remain anonymous and/or has found other available reporting mechanisms to be ineffective. Research Personnel may also address their research compliance-related questions or concerns to the Director of Research Compliance at 402-280-2511.

Creighton University