Electronic engineering
Engineering high performance electronic products that prioritise safe user interaction and power management.
We specialise in the development of electronics hardware, seamlessly integrated with industrial and mechanical design. Our deliverables span a range of applications, including biofeedback systems and advanced sensor and measurement technologies.
Our team has broad expertise in risk management and compliance for highly regulated industries. We work closely with clients to navigate complex regulatory environments, ensuring that products meet the highest standards of safety, performance, and certification. From early-stage prototyping through to full-scale production and regulatory approval.
High performance
electronics
Delivering results through what we do best...
Electronics
hardware
Embedded
systems
PCB
design
Wireless
communication
IoT/
IoMT
Schematic
capture
Electromagnetic
compatibility (EMC)
Power integrity
analysis
SPICE
simulation
Design for
manufacture (DFM)
Design for test
(DFT)
Prototype /
test
What is essential to building successful products?
We work closely with our clients, maintaining full transparency from day one. Our proven process is not guesswork, but built on rigorous standards that guide every step from the start.
Before moving into technical development, we define the concept in detail, establishing key requirements, optimising user experience, manufacturing strategy, and necessary studies.
Our goal is to minimise uncertainties and reduce risk early in the process, setting the stage for a successful and reliable product.
Our expert team focuses on these core activities:
Understand User needs, pain points & Opportunities
By collaborating with a UX team early on, we conduct user research to uncover who the users are, how they interact with the product, and where they use it. These insights reveal pain points and potential risks - so we can solve problems before they happen.
By identifying these issues upfront: we design smarter, safer solutions from the start - saving time, money and reducing rework.
Analyse, Identify and Mitigate Usability Risks
We often begin with a draft IFU (Instructions for use) to map out how the product is, or would be used in real-world settings. This early step helps inform risk management by revealing potential hazards and critical tasks. Our team collaborates to define effective risk controls, including user interface specifications.
The goal: create clear, actionable solutions that keep risk within acceptable limits.
Design, Test, Refine -Repeat
By exploring multiple design options and testing early concepts through formative evaluations, we uncover what works and what doesn’t. This ensures medical devices are not only safe, but also intuitive, efficient, and aligned with how people actually use them.
These evaluations go beyond the product itself. They help refine instructional materials and training tools - like the Instructions for Use (IFU). which are essential parts of the user interface. By testing how users interact with these materials, we make sure the entire experience supports safe and successful use.
The result: well-informed design decisions, reduced risk, and products that truly support users from first interaction to daily use.
We’re committed to your product safety and quality assurance.
We help ensure your medical device meets the necessary regulatory requirements for FDA approval by applying rigorous human factors engineering principles throughout the development process.
As an ISO 13485 certified organisation, we adhere to internationally recognised quality management standards, reinforcing our commitment to safety, usability, and compliance. Our approach minimises risk, accelerates time to market, and supports successful regulatory submissions
