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FDA QMSR Webinar Answers Common Industry Questions About the New Rule
Medical device manufacturer uses software on tablet to monitor quality and production. Image for FDA QMSR webinar recap answering common questions about the new QMSR rule.
FDA Compliance

FDA QMSR Webinar Answers Common Industry Questions About the New Rule

January 08, 2026 4 min read
Know the Facts About Software Validation in 2026
Three software engineers looking at tablet and laptop with colorful grid in background. Software validation best practices 2026.
QT9 ERP

Know the Facts About Software Validation in 2026

December 30, 2026 5 min read
FDA QMSR Inspection Readiness for 2026 and Beyond
A man and woman in lab coats are standing in lab discussing compliance with the FDA's new Quality Management System Regulation QMSR for medical devices.
Medical Device

FDA QMSR Inspection Readiness for 2026 and Beyond

December 11, 2025 5 min read
Adverse Events & Drug Reactions: The Difference & Why It Matters
Lab workers holding a tablet learn difference between adverse events and adverse drug reactions and how QT9 QMS can help reporting to FDA and other regulators
Pharma

Adverse Events & Drug Reactions: The Difference & Why It Matters

November 07, 2025 8 min read
QMS Software Validation: Ensuring FDA & ISO Compliance
Use pre validated QMS software for more efficient regulatory compliance.
FDA Compliance

QMS Software Validation: Ensuring FDA & ISO Compliance

June 04, 2025 7 min read
From Concept to Market: FDA Approval Process for Medical Devices
Medical Device

From Concept to Market: FDA Approval Process for Medical Devices

November 04, 2024 6 min read
Data Integrity: A Critical Component of FDA and ISO 13485 Compliance
FDA Compliance

Data Integrity: A Critical Component of FDA and ISO 13485 Compliance

October 08, 2024 5 min read
FDA 483 Warning Letter Guide for Life Sciences Manufacturers
FDA Compliance

FDA 483 Warning Letter Guide for Life Sciences Manufacturers

June 13, 2024 3 min read

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