The Dot Compliance Blog
Your source for AI, quality, and compliance updates, insights and best practices across the life sciences industry.
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21 CFR Part 11AnnouncementArtificial IntelligenceAudit ManagementBest PracticesBiotechnologyCAPAChange ManagementClinicalComplaint ManagementCosmeticsData and AnalyticsDocument ManagementeQMSISO 13485Life SciencesManufacturingMedical DevicePharmaceuticalQuality 4.0Regulatory ComplianceRisk ManagementSaaSTraining Management
What are the 7 Principles of a QMS?
May 2025
Beyond Compliance: The Importance of Medical Device Verification
May 2025
Does the FDA Test Medical Devices?
May 2025
Why Is Audit Readiness Easier with an AI-Powered eQMS?
May 2025
How Do I Choose the Right QMS for my Biotech Startup?
May 2025
What Is an eQMS and Why It’s Critical in Life Sciences
May 2025
The Four Pillars of a Quality Management System in the Life Sciences Industry
April 2025
Understanding the 4 Types of QMS Standards in the Life Sciences Industry
April 2025
7 Essential Steps to Implementing a QMS in the Life Sciences Industry
April 2025
What is a Quality Management System (QMS) in the Life Sciences Industry?
April 2025
ISO 13485 vs. ISO 14971: Understanding Key Medical Device Standards
March 2025
The Role of BMR and BPR in Pharma
March 2025