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
• Maintenance and tracking
• Close out audits
Please fill out the form to download our webinar "Maintaining Regulatory Compliance with Trial Documents".