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Stay informed and ahead of the curve with Trinity M Consulting's expert perspectives and industry knowledge.


Navigating Market Entry in the USA: Essential Regulatory Strategies and How OneGlobal Trinity M Consulting Can Help
Navigating Market Entry in the USA: Essential Regulatory Strategies and How OneGlobal Trinity M Consulting Can Help
Sep 3, 20243 min read

OneGlobal Trinity M Consulting: Driving Success Through Expertise, Innovation, and Passion
OneGlobal Trinity M Consulting: Driving Success Through Expertise, Innovation, and Passion
Aug 22, 20242 min read

Bringing Products to Market Globally: How OneGlobal Trinity M Consulting Leads the Way in Compliance and Regulatory Success
Bringing Products to Market Globally: How OneGlobal Trinity M Consulting Leads the Way in Compliance and Regulatory Success.
Aug 19, 20243 min read


Orphan Drug Designation (ODD): An overview and Helpful Steps to Application
Orphan Drug Designation (ODD): An overview and Helpful Steps to Application.
Aug 2, 20244 min read

Supporting Biologic Companies Navigating Regulatory, Clinical, and Quality Challenges
Supporting Biologic Companies Navigating Regulatory, Clinical, and Quality Challenges
Aug 1, 20243 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


OneGlobal Trinity M Consulting Tailored CRO Services
OneGlobal Trinity M Consulting Tailored CRO Services
Jul 10, 20243 min read


The FDA’s Final Rule on Laboratory Developed Tests (LDTs): What it Means for Clinical Laboratories
The FDA’s Final Rule on Laboratory Developed Tests (LDTs): What It Means for Clinical Laboratories
Jul 8, 20242 min read

Finding the Right Consulting Company: Your Path to Success with OneGlobal Trinity M Consulting
Finding the Right Consulting Company: Your Path to Success with OneGlobal Trinity M Consulting.
Jul 8, 20243 min read

Understanding the Differences Between 510(k) and PMA
Understanding the Differences Between 510(k) and PMA.
Jul 3, 20243 min read


How to Successfully Obtain Regulatory Approval for an OTC Product: Navigating FDA Requirements
How to Successfully Obtain Regulatory Approval for an OTC Product: Navigating FDA Requirements
Jul 1, 20243 min read


Navigating the Regulatory Requirements for Obtaining CE Marking for Medical Devices
Navigating the Regulatory Requirements for Obtaining CE Marking for Medical Devices
Jun 26, 20243 min read


Medical Device Submission to Health Canada: Helpful Reminders
Medical Device Submission to Health Canada: Helpful Reminders
Jun 24, 20242 min read


Remote Global Consulting: Benefits and Trinity M Consulting Expertise
In today's dynamic business landscape, remote consulting has emerged as a vital resource for companies seeking expertise and guidance...
Jun 18, 20243 min read


Best Practices for Obtaining FDA Approval for Medical Devices
Best Practices for Obtaining FDA Approval for Medical Devices.
Jun 12, 20243 min read


Best Practices for Creating and Maintaining a Quality Management System
Best Practices for Creating and Maintaining a Quality Management System.
Jun 10, 20243 min read


Bringing Medical Device Products to the US Market Efficiently: A Comprehensive Guide
Bringing a medical device to the US market is a complex process that requires expertise.
Jun 3, 20244 min read


Establishing a Medical Device Facility: Helpful considerations.
Establishing a Medical Device Facility: Helpful considerations.
May 31, 20243 min read


Navigating Recent Regulatory Changes: Impact on Manufacturers
Navigating Recent Regulatory Changes: Impact on Manufacturers.
May 29, 20243 min read


Successfully Submitting a New NDA Under eCTD Version 4.0
Successfully Submitting a New NDA Under eCTD Version 4.0.
May 23, 20243 min read
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