How to Improve Your Site Compliance

Many clinical trial sites face challenges to stay compliant on a study. It is important for sites to adhere to the myriad of requirements that constitute Good Clinical Practices (GCP). Sites must execute their studies in a fully compliant manner while dealing with many other activities as part of their primary jobs, and the tasks associated with the clinical study.

In this guide, we:

  • Break down the most common site violations, and reasons for protocol deviation
  • Discuss tactics and strategies to help your site team overcome these common challenges

Download our eBook: How to Improve Your Site Compliance

Who should watch?

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CEU Credits

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Certificate of Attendance

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Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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