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
The FDA Has Issued its Final Rule on QMSR; Adopts ISO 13485
February 2024
What Is an eQMS? (and Why Life Sciences Organizations Need One)
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
4 steps to speed value and minimize risk when deploying AI in quality management
April 2023
5 ways AI will change the life science industry
March 2023