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

Understanding IVDR Technical Documentation Requirements for In Vitro Diagnostic Devices (IVDs)
Understanding IVDR Technical Documentation Requirements for In Vitro Diagnostic Devices (IVDs)
Nov 11, 20245 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, 20244 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
Nov 3, 20243 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 29, 20244 min read

Conducting an Effective Regulatory Strategy
Conducting an Effective Regulatory Strategy...
Oct 10, 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, 20244 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...
Oct 5, 20243 min read

Preparing for FDA Pre-Submission and 513(g) Requests
Preparing for FDA Pre-Submission and 513(g) Requests.
Sep 12, 20243 min read


Steps to Enter the European Market
Steps to Enter the European Market.
Sep 12, 20243 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


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


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 15, 20243 min read


The Importance of Medical Writing in Regulatory Submissions
The Importance of Medical Writing in Regulatory Submissions.
Aug 13, 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


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


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
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