Abstract

BackgroundWith the growing amount of clinical research, regulations and research ethics are becoming more stringent. This trend introduces a need for quality assurance measures for ensuring adherence to research ethics and human research protection beyond Institutional Review Board approval. Audits, one of the most effective tools for assessing quality assurance, are measures used to evaluate Good Clinical Practice (GCP) and protocol compliance in clinical research. However, they are laborious, time consuming, and require expertise. Therefore, we developed a simple auditing process (a screening audit) and evaluated its feasibility and effectiveness.MethodsThe screening audit was developed using a routine audit checklist based on the Severance Hospital’s Human Research Protection Program policies and procedures. The measure includes 20 questions, and results are summarized in five categories of audit findings. We analyzed 462 studies that were reviewed by the Severance Hospital Human Research Protection Center between 2013 and 2017. We retrospectively analyzed research characteristics, reply rate, audit findings, associated factors and post-screening audit compliance, etc.ResultsInvestigator reply rates gradually increased, except for the first year (73% → 26% → 53% → 49% → 55%). The studies were graded as “critical,” “major,” “minor,” and “not a finding” (11.9, 39.0, 42.9, and 6.3%, respectively), based on findings and number of deficiencies. The auditors’ decisions showed fair agreement with weighted kappa values of 0.316, 0.339, and 0.373. Low-risk level studies, single center studies, and non-phase clinical research showed more prevalent frequencies of being “major” or “critical” (p = 0.002, < 0.0001, < 0.0001, respectively). Inappropriateness of documents, failure to obtain informed consent, inappropriateness of informed consent process, and failure to protect participants’ personal information were associated with higher audit grade (p < 0.0001, p = 0.0001, p < 0.0001, p = 0.003). We were able to observe critical GCP violations in the routine internal audit results of post-screening audit compliance checks in “non-responding” and “critical” studies upon applying the screening audit.ConclusionsOur screening audit is a simple and effective way to assess overall GCP compliance by institutions and to ensure medical ethics. The tool also provides useful selection criteria for conducting routine audits.

Highlights

  • With the growing amount of clinical research, regulations and research ethics are becoming more stringent

  • Seeing an unmet need for measures with which to ensure quality compliance by research organizations, we developed a “screening audit” that confirms whether trial documents have been properly set aside and whether all active protocols are being adhered to: it does this without interviews or source document verification

  • Development of the screening audit This study was conducted as a preliminary exploratory study through which to introduce the screening audit and to provide information on its effectiveness based on data from a single institution

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Summary

Introduction

With the growing amount of clinical research, regulations and research ethics are becoming more stringent. One of the most effective tools for assessing quality assurance, are measures used to evaluate Good Clinical Practice (GCP) and protocol compliance in clinical research. They are laborious, time consuming, and require expertise. Good Clinical Practice (GCP) is an international scientific and ethical quality standard for designing, conducting, recording, and reporting clinical research using human participants. It originated from the Declaration of Helsinki [1]. An audit is a systematic monitoring method used to determine whether clinicalresearch-related activities and documents are adequately obtained according to the approved protocol, GCP, and the applicable regulatory requirements

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