Engineering

We bring together the essential engineering concentrations 

 

We bring together the engineering concentrations necessary to design and develop medical devices successfully. This includes mechanical engineering, electrical engineering, systems engineering, software engineering, and process engineering to support Design for Manufacturability (DFM).

Mechanical Engineering

We design and develop the physical components of medical devices, including mechanisms and materials, which ensure structural integrity, functionality, and manufacturability of the device.

Electrical Engineering

We design and develop the electronic systems and components of medical devices, including circuit design, power management, and integrating components that interact with the physical world, like sensors and actuators.

Systems Engineering

We provide systems engineering, which enables the integration and coordination of all components and subsystems within a medical device. This includes requirements analysis, system integration, and system verification and validation.

Software Engineering

We develop the software that controls medical devices and processes data, including embedded software, user interfaces, and secure and efficient data management.

Process Engineering

We optimize device designs for manufacturability to facilitate manufacturing processes that are scalable, reliable, and efficient.

What's the ROI on Better Product Development?

 

Better design and development drive measurable outcomes. Organizations that achieve improved product development enhance quality through better device usability and functionality, reduce the cost of product development and cost of goods sold, accelerate time to market for product launches and future product iterations, and increase innovation with more protectable intellectual property.

Materials Engineering

We provide recommendations for off-the-shelf or custom materials and materials processing techniques that are appropriate to each application. 

Packaging & Labeling Design

We support the development, sourcing, and validation of primary, secondary, and tertiary packaging, labeling, and instructions for use according to quality and regulatory requirements for pre-clinical, clinical, and commercial stages. 

Our Approach

We simplify complex design and development challenges 

 

We help biomedical innovators understand complex challenges and create simply effective solutions. From concept generation and product brand strategy, industrial design and product development to verification and validation, we help commercialize biomedical innovations with our design and development services. 

Discovery

 

We begin by understanding where you are today, what you already have in place, and your future objectives. We accomplish this in one or two discovery meetings.

APPROXIMATE TIMING: 1-2 DAYS

 

Assessment

 

We create a written assessment summarizing where you are today and a high-level plan outlining our recommended steps to meet your future objectives.

 

Approximate Timing: 1 week

 

Statement of Work

 

We develop a detailed statement of work for the first phase of your project. The statement of work outlines the project timeline, deliverables, cost, and key milestones.

 

Approximate Timing: 1-2 weeks

 

Content Card - Just Mighty - Design - Two Color - Full (1920 x 1080)
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Your innovation Just Might change the world. But is your design up to the task? We help you turn Just Might into Just Mighty.