Orphan Drug Designation (ODD): An overview and Helpful Steps to Application
Orphan Drug Designation (ODD): An overview and Helpful Steps to Application.
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Blog
Stay informed and ahead of the curve with Trinity M Consulting's expert perspectives and industry knowledge.
Aug 13 min read
Supporting Biologic Companies Navigating Regulatory, Clinical, and Quality Challenges
Supporting Biologic Companies Navigating Regulatory, Clinical, and Quality Challenges
Jul 292 min read
Explore OneGlobal Trinity M Consulting Quality Services
Explore OneGlobal Trinity M Consulting Quality Services.
Jul 153 min read
Revolutionizing Oncology Research: The Rise of Decentralized Clinical Trials
Revolutionizing Oncology Research: The Rise of Decentralized Clinical Trials
Jul 103 min read
OneGlobal Trinity M Consulting Tailored CRO Services
OneGlobal Trinity M Consulting Tailored CRO Services
Jul 82 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 83 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 33 min read
Understanding the Differences Between 510(k) and PMA
Understanding the Differences Between 510(k) and PMA.
Jul 13 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
Jun 263 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 263 min read
OneGlobal Trinity M Consulting and Dawa Medical: A Partnership for Innovation and Excellence
OneGlobal Trinity M Consulting and Dawa Medical: A Partnership for Innovation and Excellence
Jun 242 min read
Medical Device Submission to Health Canada: Helpful Reminders
Medical Device Submission to Health Canada: Helpful Reminders
Jun 183 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 123 min read
Best Practices for Obtaining FDA Approval for Medical Devices
Best Practices for Obtaining FDA Approval for Medical Devices.
Jun 103 min read
Best Practices for Creating and Maintaining a Quality Management System
Best Practices for Creating and Maintaining a Quality Management System.
Jun 34 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.
May 313 min read
Establishing a Medical Device Facility: Helpful considerations.
Establishing a Medical Device Facility: Helpful considerations.
May 293 min read
Navigating Recent Regulatory Changes: Impact on Manufacturers
Navigating Recent Regulatory Changes: Impact on Manufacturers.
May 242 min read
OneGlobal Trinity M Consulting at FIME 2024!
OneGlobal Trinity M Consulting at FIME 2024!
May 233 min read
Successfully Submitting a New NDA Under eCTD Version 4.0
Successfully Submitting a New NDA Under eCTD Version 4.0.
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- Feb 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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