Who We Are
MATRIX MEDICAL CONSULTING is a medical regulatory and clinical affairs consulting company specializing in regulatory sciences, clinical trials, and quality systems for the medical device industry worldwide.
We are focused specifically on medical devices and combination products containing a medical device component.

Our specialties are FDA and global submissions, development and management of international clinical trials, and FDA inspections.
Our specialty is providing semi-virtual networks for conducting domestic and global clinical trials. We firmly believe this is the new business model that allows trials to run lean and minimize costs.
We have a business perspective and know economics drives multinational submissions.

What We Do
We create cost-effective, realistic and timely strategic plans for regulatory approvals and then implement and manage them through all product phases - from conception to completion. We develop a unique regulatory strategy for each product, including a step-by-step pathway to approval.

We use our knowledge of the unique requirements of national and international agencies to efficiently prepare regulatory strategies, clinical studies and their respective submissions.

We have the expertise to integrate scientific, medical, regulatory and clinical practice concepts and requirements into a single program for your product.