Research Quality Assurance Program

Drexel University’s Office of Research & Innovation (ORI) is committed to maintaining the highest standards of quality and research compliance consistent with best practices for quality, integrity, and regulatory requirements of research conducted by Drexel University.

The Research Quality Assurance Program conducts research quality assurance reviews or audits at Drexel University. The intent of the reviews is to evaluate compliance with applicable laws and regulations, institutional policies and procedures, guidelines, funder requirements, and approved protocols, as applicable under the ORI. Reviews may include but are not limited to human subject research, animal research, research integrity, conflict of interest, export compliance, and as requested by the Institutional Official (IO).  
 
Continuing oversight of research activities is required by federal laws, regulations, policies and guidelines. Quality assurance reviews ensure compliance with the regulatory and ethical standards governing research activities, as well as guide the University in identifying opportunities for improvement and provide recommendations on how to achieve improvement. Quality assurance reviews also support ongoing education and training initiatives of the ORI. 
 
Quality assurance reviews promote regulatory compliance as well as facilitate communication and collaboration between researchers and the ORI, promoting a culture of compliance institution wide. Some benefits that may be gained from quality assurance reviews, include, but are not limited to:  

  • Increased understanding of the regulations that guide research projects and procedures.  
  • Increased communication concerning Federal regulations and University policies.  
  • Access to an individual to clarify the Federal regulations and University policies.

Additional Information

The Research Quality Assurance Program can assist with setting up systems and processes at the beginning of a trial to validate all regulatory requirements and essential documents are in place (i.e., documentation of investigators qualifications, confirming Delegation logs are accurately completed, assisting with training documentation).

During the study, the Research Quality Assurance Program can work with the study team in doing an informal review to check for compliance. Once completed, any findings are reviewed with the study team. 

The Research Quality Assurance Program will also conduct routine post-approval reviews of research or research activities at Drexel University. These internal reviews are intended to help investigators assess compliance with all applicable federal and state laws, regulations, institutional policies, and guidelines.

In addition, a directed or for-cause review may be conducted as requested by the Institutional Official, IRB, IACUC, or other regulatory office. Refer to the procedures: ORI-601 Research Quality Assurance Reviews found in the ORI Compliance Catalog for more information on quality assurance reviews. 

An inspection, in the context of clinical research, involves a thorough examination of the research processes, documentation, and compliance with applicable laws and regulations. These inspections are conducted by agencies such as the Food and Drug Administration (FDA), Department of Justice (DOJ), National Institutes of Health (NIH), Drug Enforcement Administration (DEA), European Medicines Agency (EMA), Health Canada, and other regulatory bodies.

The Research Quality Assurance Program can assist with agency inspections, including inspection preparation for personnel, documentation review and organization, taking notes during the inspection, and assisting with responses at the end of the inspection.

If you are notified of any inspection, please email Marisa Corbett at mjc535@drexel.edu.

The Research Quality Assurance Program can provide support to investigators during sponsor-conducted independent audits, which are distinct from routine monitoring visits. This support includes evaluating compliance with the study protocol, Standard Operating Procedures (SOPs), ICH E6 R2 Good Clinical Practices, ICH E6 R3 Good Clinical Practices [PDF] (released January 6, 2025), and any applicable regulatory requirements.

The Research Quality Assurance Program can assist in organizing necessary documentation, preparing for the audit, and addressing any findings or recommendations from the sponsor to ensure the study meets all required standards.

Marisa Corbett

Marisa Corbett

Executive Director for Research Quality Assurance
Research Compliance