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.

Introduction

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