Monitoring & Auditing

Our audit team conducts both remote and on-site monitoring and auditing visits to ensure protocol adherence, participant safety, data integrity, and site readiness.

Overview

Meeting Industrial Standards

Monitoring and auditing during study conduct protect participant safety and data integrity. Frontier Science research processes and procedures are compliant with applicable regulations and industry standards.

Tailored Monitoring and Auditing

Frontier Science provides services in overseeing study monitoring, and assessing sites for overall compliance with study-specific processes.

Study Monitoring

Site Assessments

Frontier Science can tailor a monitoring or auditing team based on the requirements of the specific study and the work flows that need to be reviewed by a third party.

Risk-Based Strategies

Our risk-based strategy focuses on those trial processes most likely to affect participant safety and data integrity so that investigators and sponsors can quickly and effectively mitigate risks or address errors. This adaptive approach identifies the critical areas that require improvement and provides benefits in quality, timelines, and cost.

Identify Risks of Trial

Develop Key Performance Indicators

Gauge Trial Performance

Track Standards & Best Practices

We have developed a web-based system that generates and stores monitoring and audit reports, and where corrective and preventive action plans can be assigned and electronically signed.

Our Audit Team

We have developed a web-based system that generates and stores monitoring and audit reports, and where corrective and preventive action plans can be assigned and electronically signed.

Frontier Science ensures that your assigned team members are given adequate tools and training to promote the success of the trial.

  • We provide assessments for overall site compliance with study-specific processes, remotely or on-site

  • Participating entities are assessed on their general adherence to Good Clinical Practice (GCP) guidelines

  • We focus on trial processes most likely to affect participant safety and data integrity to effectively mitigate risks or errors