5 Reasons Your TMF Isn’t Inspection-Ready
(and what you can do to fix it)

Learn to Avoid the Most Common Inspection-Readiness Mistakes

Complete the brief form on this page to download the new guide from Phlexglobal, “5 Reasons Your TMF Isn’t Inspection-Ready (and what you can do to fix it).”

Based on helping companies pass hundreds of inspections by regulatory agencies worldwide, the guide will help you identify and correct those areas most often flagged by inspectors, including:

• Lack of essential documents in the TMF required to enable the reconstruction of trial events and demonstrate compliance
• Inability of sponsors to demonstrate effective oversight of clinical trial activities to fulfil their regulatory obligations
• Insufficient functionality in the eTMF system used