The FDA cited hundreds of companies last year for this problem. Solving this problem is as simple as setting up automated workflows within your Quality Management System (QMS) or FDA Compliance Management System.
You can create different workflow templates for various types of events such as complaints, non conformances and equipment issues, ensuring:
• Automatic routing of corrective actions through review, root cause analysis, action taken and verification.
• Escalation of overdue corrective actions to supervisors when key milestones are overdue.
• Effective prioritization and handling of corrective action requests through risk-based filtering and final verification.
