Clinical trial sites face many challenges to staying compliant on a study.

Consider for instance...

• Site staff deal with a lot of activities as part of their primary jobs, and the tasks associated with conducting a clinical research study are often considered extra work
• There are many different factors to manage and demands on the site during a trial
• Sites often deal with multiple trials
• Clinical trial protocols have become increasingly complex

These and other factors can make it difficult for sites to adhere to the myriad of requirements that constitute Good Clinical Practice (GCP). Yet, this is no excuse. Sites must execute these studies in a fully compliant environment.

In this guide, we break down the most common site violations, and reasons for protocol deviation. Then, we discuss tactics and strategies to help your site team overcome these common challenges and negative outcomes.

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