Blog2025-03-18T10:11:14+00:00

AssurX Blog

Straight talk for regulated industries.

1706, 2025

QMS Software: When to Configure and When to Customize

June 17th, 2025|Archives, eMDR, FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management, SaaS & Cloud Computing|

When it comes to managing quality and compliance in today’s regulated industries, selecting the right enterprise QMS software is a strategic decision. Many vendors claim their QMS soft [...]

1006, 2025

Why QMS Software Is No Longer Optional in Regulated Industries

June 10th, 2025|FDA Regulated Industries, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

Many companies are still clinging to paper-based and unconnected electronic processes, despite the clear disadvantages. Without modern tools like QMS software, these organizat [...]

2105, 2025

Human Factors in CAPA Part III: How To Secure Management Commitment

May 21st, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

In the third and final part of our Human Factors in CAPA series, we’re tackling the big one: management commitment. Why is it so important? Because getting your leaders truly committe [...]

1405, 2025

Human Factors in CAPA Part II: How to Improve CAPA Accountability

May 14th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

In Part I of our Human Factors in CAPA series, we talked about employee engagement and its importance to a strong CAPA program. Today, we’re shifting gears to explore another essentia [...]

705, 2025

Human Factors in CAPA Part I: How to Improve Employee Engagement

May 7th, 2025|FDA Regulated Industries, Food & Beverage Industry, Manufacturing Industries, Medical Device Industry, Pharmaceutical Industry, Quality Management|

At its core, corrective and preventive action (CAPA) is about systematically evaluating problems and enacting permanent solutions that minimize risk—for both customers and the busines [...]

2304, 2025

Top 5 Challenges When Preparing for a NERC Audit (And How to Overcome Them)

April 23rd, 2025|Energy & Utilities Industry, NERC Compliance, Regulatory Compliance Management|

Preparing for a NERC (North American Electric Reliability Corporation) audit can be daunting for any registered entity. With evolving standards, complex infrastructure, and a high bar [...]

Go to Top