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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, 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
Nov 3, 20244 min read
Best Practices for Updating Your Medical Device File
Best Practices for Updating Your Medical Device File...
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 1, 20243 min read
Navigating the Regulatory Pathway for Selling Class II Medical Devices in Canada
Navigating the Regulatory Pathway for Selling Class II Medical Devices in Canada...
Sep 30, 20244 min read
Tips for Creating a Regulatory Pathway for a Medical Device to be Sold in the USA
Navigating the regulatory landscape for bringing a medical device to market in the US can be challenging but essential to product safety...
Sep 26, 20244 min read
The Benefits of Partnering with a Consulting Firm: Why It’s the Smart Choice for Businesses
The Benefits of Partnering with a Consulting Firm: Why It’s the Smart Choice for Businesses
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 20, 20244 min read
The Importance of Medical Writing for Regulatory Submissions
In the fast-paced pharmaceutical, medical device, and biotechnology industries, effective communication is critical to success.
Sep 19, 20242 min read
Navigating FDA Requirements for Combination Products and Post-Market Reporting
Combination products, which integrate medical devices with drugs or biologics, are subject to stringent FDA regulations.
Sep 12, 20243 min read
Navigating the Complex World of Regulatory Approval: A Step-By-Step Guide for Success
Navigating the Complex World of Regulatory Approval: A Step-By-Step Guide for Success
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 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.
Aug 1, 20243 min read
Supporting Biologic Companies Navigating Regulatory, Clinical, and Quality Challenges
Supporting Biologic Companies Navigating Regulatory, Clinical, and Quality Challenges
Jul 27, 20243 min read
Navigating the Transition to QMSR with OneGlobal Trinity M Consulting
Navigating the Transition to QMSR with OneGlobal Trinity M Consulting.
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