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 to Know about IEC 62304 and Why It’s Important for SaMD
March 2024
The Impact of Generative AI in the Life Sciences Industry
February 2024
The FDA Has Issued its Final Rule on QMSR; Adopts ISO 13485
February 2024
What Is an eQMS? A Complete Guide for Life Sciences
February 2024
Revolutionizing Complaint Management in Medical Device with AI-Powered Quality Management Software
January 2024
Raising the Bar in Medical Device Compliance with Dot Compliance
December 2023
Navigating FDA Compliance: A Guide to 21 CFR Part 210 and Part 211
November 2023
Unlocking Success: How the Right eQMS Can Be a Game Changer
September 2023
The Evolution of Document Management Systems
September 2023
How to Choose the Right eQMS – The Ultimate Guide
August 2023
CAPA in the Age of Generative AI
May 2023
How the use of AI is impacting life sciences manufacturing
April 2023