Best Practices for Investigating Quality Deviations

Learn about the Best Practices for Investigating Quality Deviations that will help you manage any audits that come your way.
The COVID-19 pandemic has left a growing backlog of delayed inspections in its wake, and the FDA is prepared to hire additional employees and significantly increase the rate of inspections to compensate. That means an increased likelihood of your organization facing an audit, and increased importance in having an effective strategy for investigating quality deviations.
MasterControl has partnered with regulatory experts Regulatory Compliance Associates (RCA) for an exclusive virtual event exploring best practices for investigating quality deviations. Join Sue Schniepp - RCA Distinguished Fellow for an informative event designed to help you manage quality events and effectively manage any audits that come your way.
We’ll explore strategies for:
Audit management and how to define root cause early.
Why centralized workspaces are interconnected with quality.
CAPA processes and quality event forms.
Answering interview questions about standardization.
Organizing source documents for audit reporting