FSVP Violations Under Fire: FDA’s 2025 Warning Letters and the Listeria Outbreak Exposing Global Food Supply Chain Risk
In 2025, the U.S. Food and Drug Administration (FDA) has continued its crackdow [...]
9
10, 2025
22
09, 2025
Building a Strong EQMS Foundation: Why Document Control and Training Come First
When organizations implement an enterprise quality management system (EQMS), th [...]
23
07, 2025
Why Quality Audits Are Critical for Compliance in FDA and ISO Environments
Quality audits are a cornerstone of compliance in FDA and ISO-regulated environ [...]
25
06, 2024
12 Strategies for Successful CAPA Management
There’s no question about it: should an auditor or inspector visit your facilit [...]
13
06, 2024
Customer Quality Management: How the QMS Can Help
Customer complaints are a fact of life in any industry. Even though manufacture [...]
29
05, 2024
The Power of Change Management Tools
Look through even a few FDA warning letters, and you’re likely to find violation [...]
9
05, 2024
Validation Lifecycle Management System Essentials: What to Know
To test or not to test? The truth is, there really is no question. Whether you’r [...]
18
04, 2024
How Manufacturing Quality Management Systems Influence Customer Satisfaction
In the intricate world of manufacturing, pursuing quality is not just a goal bu [...]
4
04, 2024
Guide to Choosing the Right Training Management Software
An analysis of U.S. Food and Drug Administration (FDA) warning letters by the F [...]
28
03, 2024
How EHS Software Solutions Can Revolutionize Workplace Safety
According to U.S. Bureau of Labor Statistics data, the number of preventable wor [...]
