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Stay informed and ahead of the curve with Trinity M Consulting's expert perspectives and industry knowledge.
The Phases of Clinical Trials: Navigating the Path from Discovery to Approval
The Phases of Clinical Trials: Navigating the Path from Discovery to Approval
Nov 3, 20243 min read
Understanding Regulatory, Quality, and Post-Market Requirements for OTC Drug Submissions: U.S. and India
In this blog, we will outline the key requirements for OTC drug submissions in both the U.S. (FDA) and India.
Sep 24, 20244 min read
Leveraging Real-World Evidence (RWE) for Clinical Submissions: A Strategic Approach
Leveraging Real-World Evidence (RWE) for Clinical Submissions: A Strategic Approach.
Sep 3, 20245 min read
Revolutionizing Oncology Research: The Rise of Decentralized Clinical Trials
Revolutionizing Oncology Research: The Rise of Decentralized Clinical Trials
Jul 15, 20243 min read
OneGlobal Trinity M Consulting Tailored CRO Services
OneGlobal Trinity M Consulting Tailored CRO Services
Jul 10, 20243 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
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
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
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
The Essentials of Electronic Common Technical Document (eCTD) Submissions: A Guide for Regulatory Affairs Professionals
The Essentials of Electronic Common Technical Document (eCTD) Submissions: A Guide for Regulatory Affairs Professionals
Apr 16, 20243 min read
Streamlining Global Regulatory Submissions: Guide
In the rapidly evolving landscape of healthcare and medical technology, navigating the complex web of global regulatory requirements is a...
Mar 18, 20243 min read
Challenges of Decentralized Clinical Trials: Navigating the Future of Clinical Research
Introduction: Decentralized clinical trials (DCTs) offer significant potential to revolutionize the clinical research landscape by...
Mar 5, 20242 min read
Navigating the Path to Regulatory Approval: Preparing an eCTD Submission for a New Drug in the US
Introduction: The process of bringing a new drug to market involves numerous steps, with one critical milestone being the submission of a...
Feb 28, 20242 min read
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- 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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