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Blog
Stay informed and ahead of the curve with Trinity M Consulting's expert perspectives and industry knowledge.
Nov 11, 20245 min read
Understanding IVDR Technical Documentation Requirements for In Vitro Diagnostic Devices (IVDs)
Understanding IVDR Technical Documentation Requirements for In Vitro Diagnostic Devices (IVDs)
Nov 3, 20244 min read
OneGlobal Trinity M Consulting Uses ISO 9001 and ISO 27001 to Provide the Best Consulting Services for Medical Device, Biotech, and Pharma Companies
How OneGlobal Trinity M Consulting Uses ISO 9001 and ISO 27001 ...
Nov 3, 20243 min read
The Phases of Clinical Trials: Navigating the Path from Discovery to Approval
The Phases of Clinical Trials: Navigating the Path from Discovery to Approval
Oct 29, 20244 min read
Tips for Successful New Product Development in the Medical Device Industry
Tips for Successful New Product Development in the Medical Device Industry
Oct 10, 20244 min read
Conducting an Effective Regulatory Strategy
Conducting an Effective Regulatory Strategy...
Oct 5, 20244 min read
Effective Strategies for Conducting a Gap Assessment in Life Sciences
Effective Strategies for Conducting a Gap Assessment in Life Sciences...
Oct 5, 20243 min read
The Power of Project Management in Life Sciences and How OneGlobal Trinity M Consulting Can Help
The Power of Project Management in Life Sciences and How OneGlobal Trinity M Consulting Can Help...
Sep 24, 20244 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 12, 20243 min read
Preparing for FDA Pre-Submission and 513(g) Requests
Preparing for FDA Pre-Submission and 513(g) Requests.
Sep 3, 20245 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, 20243 min read
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
Aug 22, 20242 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 19, 20243 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 15, 20243 min read
How OneGlobal Trinity M Consulting Empowers Venture Capital & Startups with Comprehensive Consulting Services
How OneGlobal Trinity M Consulting Empowers Venture Capital & Startups with Comprehensive Consulting Services.
Aug 13, 20243 min read
The Importance of Medical Writing in Regulatory Submissions
The Importance of Medical Writing in Regulatory Submissions.
Aug 2, 20244 min read
Orphan Drug Designation (ODD): An overview and Helpful Steps to Application
Orphan Drug Designation (ODD): An overview and Helpful Steps to Application.
Jul 15, 20243 min read
Revolutionizing Oncology Research: The Rise of Decentralized Clinical Trials
Revolutionizing Oncology Research: The Rise of Decentralized Clinical Trials
Jul 10, 20243 min read
OneGlobal Trinity M Consulting Tailored CRO Services
OneGlobal Trinity M Consulting Tailored CRO Services
Jul 8, 20242 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
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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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