Medical Device Product Development is what we do...

Let us help you clear the obstacles to get your product to market.



Our multi-disciplinary regulatory, design, and engineering team is medical device focused, allowing us to help you navigate easily from concept to commercialization.
Let’s get Started
Let’s get Started

End-to-End Product Development

Multi-Disciplinary
Engineering Team
Multi-Disciplinary
Engineering Team

Our engineers and medical device developers have turned some of the most innovative designs into commercial-grade products.

Human Factors &
Industrial Design

We prioritize intuitive and safe design, integrating human factors in all phases, conducting studies to address vital user interactions and interpretations. Read More...

Software & Hardware
Development
Software & Hardware
Development

Partner with Vantage MedTech’s embedded, mobile, web, and enterprise software engineers to help you bring exciting innovations to your users.

 

Pre-clinical &
First-in-Human Systems
Pre-clinical &
First-in-Human Systems

Develop pre-clinical and first-in-human systems with precision and innovation, optimizing for successful transitions from research to human applications.

Cybersecurity
Analysis

Integrated cybersecurity allows you to prioritize secure communications, data protection, integrity, user authentication, software maintenance, physical access, and reliability.
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Verification &
Validation
Verification &
Validation

DV prototypes created during V&V undergo formal testing, including design verification, validation, and regulatory testing, documented for process validation preparation.

Every great product starts with
a great idea.

Our end to end engineering services can help you transition your vision to a market-ready and manufacturable design.

 

Our Approach

Vantage will partner with you at any phase of your product development;  we meet you where you’re at.  Our approach is to ensure a solid strategy is in place; this includes a Regulatory Strategy development or review followed by Industrial Design review for user needs and human factors.  The goal is to “measure twice and cut once” to minimize your cash burn and time to market.

Ready to Run

Once we have your consensus, we can bring our full set of engineering services and manufacturing to bear to move your product through regulatory approval, clinical success, and market introduction and acceptance.

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Explore Our Comprehensive Capabilities

Strategy and Feasibility

New Product Introduction

Manufacturing