The effective auditing of laboratory data systems is essential in order to ensure that the expectations of regulatory agencies are met. This webinar will provide details of the most common non-conformances and provide staff members, who are unfamiliar with laboratory computer systems with an understanding of the controls that are necessary to ensure the integrity of analytical data.
The webinar will teach participants the importance of correct data system configuration and what to look for during the audit. Businesses will benefit by reducing the risk of regulatory action as a result of failure to comply with current expectations.
Areas Covered in the Session :
Categories of laboratory data system (GAMP)
Lifecycle management, archiving and backup
What counts as raw data?
Protecting the integrity of analytical data
General guidance on assigning user privileges
Operating system configuration.
Application configuration
Controls appropriate for chromatography data systems
Practices that aid compliance with data integrity requirements
Examples from recent FDA warning letters
Who Should Attend:
Staff who are required to audit analytical operations who do not have a chemical QC background
Auditors who require updating on current regulatory expectations
QC staff who needs help in regulatory compliance
Staff who would like to understand the implications of data integrity for laboratory data systems