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Surgery

Usability and human factors engineering

Demonstrating safe, effective product use in intended environments.

Consistent with safety standards, FDA and other regulatory clearance requirements, Lucid’s team embeds use risk analysis, mitigation and structured use testing into new product development.
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We evidence elimination or acceptable reduction in risks of harm or degraded performance from user interactions with your system.

 

Collaborating with your product development team, or Lucid's designers and engineers, our human-centered, regulatory aware approach ensures design meets real world requirements.

Brain cancer medical device

Human factors engineering delivers:

Improved adherence

Discovering the right fit to users physiology and physical  capabilities helps our team optimise safety and performance.  

 

We aim to drive and monitor people's motivations to re-use, subscribe or repeat purchase your products and services. 

Reduced support costs

Developing simple, relatable, intuitive user interactions reduces risks of misinterpretation, misuse and user dissatisfaction.

 

Fewer support calls, fewer returns and in reduced risk of reporting to regulatory bodies drives improved margins and reputation.

Accelerated

 compliance

Our team helps simplify user interaction and demonstrate safe effective precedents in use.

 

Evidence can reduce iteration, sample size and cost of testing and the timescale of your regulatory pathway.

A regulatory complaint approach...

Usability
engineering
planning

Task
analysis
 

informal
observation
and roleplay

Usability
risk
analysis

Formative
usability
evaluations

Use
risk
mitigation

Summative
usability
studies

Human factors engineering 
reports

Mitigating risk through design

Let's imagine, design and make your future, together 

Lucid Group Limited
Unit 3, Enterprise House
Manchester Science Park
M15 6SE
England
ideas@lucidinnovation.com
+44(0)161 860 0058
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