Data Integrity and Computerized System Validations (CSV) have become an area of increased scrutiny for regulatory agencies over the last several years. Understanding how the agencies view data integrity is critical for laboratories to maintain complete compliance.
During this webinar, we investigated trends seen globally for data integrity violations and avenues for remediation. Defining how the agencies view CSV and approaching industry best practices for new instrumentation or remediation efforts to also comply with data integrity are outlined during this presentation.
In this webinar you’ll learn:
• How the FDA views data integrity
• How are CSV requirements met
Who should attend:
• Lab Supervisor/Manager/Director
• Technology Transfer, Lab QA/QC