Aubrey Group, Inc. specializes in the development and manufacture of electronic and electromechanical devices for medical use.

We provide innovative design and complete engineering services, plus prototypes, clinical builds, and full-scale production capability.

We are registered with the FDA as a Medical Device Establishment and are licensed by the California Food and Drug Branch for the design and manufacturing of medical devices. Our Quality System complies with the ISO 13485 standard.

Experience
We offer broad-based technical skills for medical design, supporting a range of clients from high-tech start-ups to established Fortune100 companies. Our staff consists of senior engineers, many with advanced degrees, experienced in the design of complex medical products.

This expertise assures development by industry-leading engineers who know what works, and practice their art constantly. The results: quick-turns in design, fewer design iterations, and fully functioning prototypes.

Rapid Development
By leveraging in-house technology and knowledge, design and fabrication of microprocessor-controlled products can be fast-tracked. Complex medical devices from concept to prototype can usually be completed in three to twelve months.

In addition, Aubrey Group streamlines documentation and data entry from initial services and confidentiality agreements through our customized MRP system. This approach has proven very successful in our fast-paced environment.

Project Management
Our management philosophy encourages a collaborative environment, where productivity demands and engineering creativity are balanced. The project manager provides weekly progress reports to budget and schedule, and remote, secure client access for project files. Emphasis is placed on customer communications with ongoing contact across all functional levels of the client’s team.

Quality Design
Our designs are safe, effective, and reliable. To meet these requirements, we analyze product risks, thoroughly specify requirements, simulate user interfaces, satisfy EMI thresholds, extensively test designs, and validate performance.

Our designs also meet the requirements of the FDA, FCC, IEC and UL and we are an FDA registered medical device manufacturer.

Manufacturing
As part of our time-to-market commitment in turnkey projects, our development team provides a seamless transition to manufacturing. This close integration means shorter lead times and better test methods, and therefore higher return on investment.

Categories this company is listed under in the North American Suppliers Directory:

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