The Dot Compliance Blog

Your source for AI, quality, and compliance updates, insights and best practices across the life sciences industry.

Can a QMS Automate CAPA Management?

Why Do Medical Device Companies Need an ISO 13485-Compliant QMS?

What QMS Features Should We Prioritize in 2025?

What Does ISO 13485 Require for a Medical Device QMS?

How Is a QMS Used in Clinical Trials?

Why Do Biotech Startups Need a QMS Early On?

What Are the Key Components of a Modern QMS?

Top Features to Look for in a Life Sciences QMS Platform

Quality as a Business Strategy: Why Compliance Alone Isn’t Enough

How to Prepare for a QMS Audit: A Step-by-Step Checklist

QMS Selection Checklist: 15 Questions to Ask Before You Buy

What’s the Difference Between a Cloud-Based and On-Premises QMS in the Pharmaceutical Industry?