How to Manage Non-Conformance with QISS QMS System?
QISS QMS provides a structured approach to managing non-conformances to ensure timely resolution and prevent recurrence. Read more.
Definition, Types & Importance of Non-Conformance
16 January, 2025
Challenges in Document Control for Quality Management
12 January, 2025
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When Should an NCR be Issued & How to Resolve It?
08 January, 2025
Common Causes of Non-conformance in the Manufacturing Sector
06 January, 2025
10 Best Practices To Build a Strong CAPA Management System
Learn 10 best practices to build a strong CAPA system that ensures quality and prevents recurring issues in your business.
How to Manage the CAPA Process with QISS QMS?
This article explores the detailed steps of the CAPA process, referencing ISO & FDA regulations. We’ll also look at how QISS QMS helps manage it.
CAPA in Regulated Industries: Meeting FDA, ISO, and Other Compliance Standards
Understanding CAPA and its role in meeting FDA, ISO, and other compliance standards is important for businesses to maintain high-quality standards.
Challenges in CAPA Management and How to Overcome Them
CAPA is an essential process for ensuring ongoing quality improvement in organizations. However, managing it effectively can be challenging. Read more.