- LCMC Site Addition Guidance (revised 12/1/2023)
- IRB Fees
- FDA Inspections
- International Conference on Harmonization - Good Clinical Practice (ICH-GCP) Applicability to Human Research Policy (revised 4/25/2023)
- HHS FWA Information
HRPP Standard Operating Procedures
Tulane University Human Research Protection Program Policies and Standard Operating Procedures (revised 5/02/2023) - These SOPs incorporate the new review categories and approval criteria as mandated by the 2018 Common Rule. Please note that additional clarifications and updates to existing Tulane policy governing Human Subject Research Protection are also contained herein. These clarifications and updates apply to ALL studies regardless of initial approval date.
Executive Summary of Revisions to the HRPP Standard Operating Procedures (dated 5/2/2023)
Executive Summary of Revisions to the HRPP Standard Operating Procedures (dated 3/1/2023)
Executive Summary of Revisions to the HRPP Standard Operating Procedures (dated 8/23/2019)
Tulane University Human Research Protection Program Policies and Standard Operating Procedures (revised 11/27/2017) - The review categories and approval criteria contained in the SOPs dated 11/27/2017 remain applicable for studies granted initial approval prior to January 21, 2019.
Executive Summary of Revisions to the HRPP Standard Operating Procedures (dated 12/4/2017)
Tulane University HRPO
1440 Canal Street, Suite 1851, TW-8436
New Orleans, LA 70112
Tel: 504-988-2665
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