Maintaining Regulatory Compliance with Trial Documents

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FDA regulations and GCP requirements necessitate that certain documents are created, maintained, revised and archived during a clinical trial. These documents need to be complete, accurate, and present at various times during the trial: initiation, mid-study, and close out. 

This Webinar will discuss how to maintain trial document compliance: 

• Regulatory document requirements 
• Templates 
• Maintenance and tracking 
• Expirations/Revisions 
• Close out audits

Please fill out the form to download our webinar "Maintaining Regulatory Compliance with Trial Documents".