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Stay informed and ahead of the curve with Trinity M Consulting's expert perspectives and industry knowledge.
Manufacturing Inspections for Medical Devices in the USA: FDA Requirements and Best Practices
Manufacturing Inspections for Medical Devices in the USA: FDA Requirements and Best Practices
Mar 173 min read
Best Practices for Maintaining a Quality Management System
In the highly regulated medical device industry, maintaining a Quality Management System (QMS) that complies with ISO 13485:2016 is crucial.
Mar 173 min read
The FDA’s Quality Management System Regulation (QMSR) Takes Effect February 2, 2026: What You Need to Know
The FDA’s Quality Management System Regulation (QMSR) Takes Effect February 2, 2026: What You Need to Know
Feb 102 min read
Effective Strategies for Conducting a Gap Assessment in Life Sciences
Effective Strategies for Conducting a Gap Assessment in Life Sciences...
Oct 5, 20244 min read
Explore OneGlobal Trinity M Consulting Quality Services
Explore OneGlobal Trinity M Consulting Quality Services.
Jul 29, 20242 min read
Navigating the Transition to QMSR with OneGlobal Trinity M Consulting
Navigating the Transition to QMSR with OneGlobal Trinity M Consulting.
Jul 27, 20243 min read
Navigating the Latest Updates to the FDA's Quality Management System Regulation (QMSR)
Navigating the Latest Updates to the FDA's Quality Management System Regulation (QMSR)
May 21, 20244 min read
Upcoming Events
- Feb 18 - Feb 20, 2025Feb 18 - Feb 20, 2025Dallas, 650 S Griffin St, Dallas, TX 75202, USAWe’re thrilled to announce that OneGlobal Trinity M Consulting will be attending the Medtrade Event at the Kay Bailey Hutchison Convention Center in Dallas, TX! 🗓️ Expo: February 19-20, 2025 🗓️ Conference: February 18-20, 2025 Join us as we connect with industry leaders, explore the latest innov
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