This session offers a U.S. Food and Drug Administration Investigator's insights from sponsor inspections that will help you to identify and prevent the problems that may arise for your data and/or application during the collection of tens to hundreds of thousands of documents during a single trial.
CEU: 1.00 ACRP
Speaker:
Lakecha Lewis, International Inspection Cadre, U.S. Food and Drug Administration
Watch a Sneak Peek into the Session Content: