AI is no longer a future concept in lifesciences, it’s actively being deployed across business processes from regulatory submissions to manufacturing monitoring to quality operations. But while ...

On April 2, 2026, the FDA issued a warning letter that should be on the desk of every Quality leader in life sciences. It cites several familiar deviations — but embedded in the findings is something ...

In highly regulated industries such as pharmaceuticals and biotechnology, manufacturing is about much more than producing a product. Companies must prove through clear documentation and testing that ...

Join us for an interactive webcast exploring how artificial intelligence (AI) is transforming manufacturing efficiency. This engaging session will highlight practical applications of AI that enhance ...

Compliance Group is proud to participate in the 2026 ISPE AI in Life Sciences Summit – Powered by GAMP®, a premier global event bringing together leaders from pharmaceutical manufacturing, regulatory ...

We’re excited to announce that Compliance Group will be attending the Realize LIVE Americas 2026 conference, happening in Detroit, Michigan from June 1–4, 2026. This premier industry event, hosted by ...

The shift from QSR to QMSR is now in full effect. The FDA has aligned 21 CFR Part 820 with ISO 13485:2016, effective Feb 2026. While this alignment eases global compliance, many MedTech companies ...

The FDA has accomplished one of the most important regulatory overhauls in decades by replacing the traditional Quality System Regulation (QSR) with the Quality Management System Regulation (QMSR).

This March, join our team who will be giving hands-on training for life science professionals. With over 55 tutorials to choose from, you are sure to walk away with new industry leading knowledge and ...

The Veeva MedTech Summit 2026 brings together innovators and leaders across the medtech industry for impactful learning, collaboration, and growth. Compliance Group is proud to be part of this ...