Blogs & Articles

Are you involved with cosmetics and are unsure of your related regulatory requirements? Does hearing about ISO 22716, US FDA 21 CFR Part...

One of the primary challenges we encounter when embarking on a CSV (Computerized System Validation) or a QSA (Quality Software Assurance)...

This is not a simple question. Much like success, talk to most people and they want to have “it”, but what does “it” mean?

If your business is building software for the Life Sciences industry, InnovX can help you do that.

The new GAMP Guidance is a must-read. Find out what changed and our first impressions of this new edition.

In this blog, we explain "Part 11", the reasons that led to the need for this regulation, and the needs for following it.

This blog will present three critical supply chain risks put forward by COVID , as well as their appropriate mitigations

This blog recaps the key differences and and touch points between entreprise, business and system architecture.

Selecting the correct Enterprise Resource Planning (ERP) software can be a daunting task. With the prevalent risks of implementation....

identifies GCP, GMP and Med Devices regs you must consider when devising an ERP validation strategy.

ERP systems are critical and complex applications. Here are 5 mistakes you should avoid when validating them.