We are Human

SERVICES

From front-end innovation to validation, discover how We are Human can support your product development process

STRATEGY & PLANNING

We combine our expertise in creative Human Centred Design with technical Human Factors Engineering principles to create a tailored approach to suit your needs.

From bigger-picture strategy facilitation to product-specific activity planning, we can support you.

We deliver:

  • Human Factors Engineering Plans & Processes
  • Human Centred Design Plans & Processes
  • Agile Design & Test Sprint Plans
  • Design & Innovation Roadmaps
  • Human Factors Standard Operating Procedures
Helping you focus and deliver

EXPLORATORY RESEARCH

We are passionate about conducting research to discover unmet needs, innovation opportunities and powerful insights. By immersing ourselves into real-world environments, listening to people’s stories, observing their behaviours and asking the right questions, we help you create genuine solutions that make an impact.

Example methods we use at this stage include:

  • Contextual Inquiry
  • Design Ethnography
  • Diary Studies
  • User Journey Mapping
  • Persona Creation
  • In-Depth Interviews 
  • Empathy Mapping

We are passionate about conducting research to discover unmet needs, innovation opportunities and powerful insights. By immersing ourselves in real-world environments, listening to people’s stories, observing their behaviours and asking the right questions, we help you create genuine solutions that make an impact.

Example methods we use at this stage include:

  • Contextual Inquiry
  • Design Ethnography
  • Diary Studies
  • User Journey Mapping
  • Persona Creation
  • In-Depth Interviews 
  • Empathy Mapping
  • Heuristic Analysis
Helping you design the right thing

INSTRUCTIONAL MATERIALS DESIGN

We design and develop effective instructional materials including:

  • Instructions for Use (IFU)
  • User manuals (UMs)
  • Quick Reference Guides (QRGs)
  • Training Manuals

We work closely with our clients to provide:

  • Styling and layout options
  • Initial “wireframe” IFU concepts
  • First & revised drafts
  • Final printed designs
  • Traceability to applicable standards

We utilise our combined experience in design, human factors and regulatory to create clear and concise instructions to support safe and effective device use.

Helping you prioritise the human experience at every step

USABILITY TESTING

From Formative to Summative/Validation testing, we have extensive experience conducting usability studies across the UK, USA and EU.

We provide end-to-end study support with:

  • Test protocol writing
  • Ethical/IRB approvals
  • Participant recruitment
  • Study logistics
  • Expert moderating
  • Data capture
  • Rigorous analysis
  • Reporting
Helping you design the thing right

USE RELATED RISK MANAGEMENT

We support comprehensive use-related risk management using our systematic approach to use-related risk identification and documentation

Our expert team can assist you with workshops and desk based activities on:

  • Known Problems Analysis (KPA)
  • Hierarchical Task Analysis (HTA)
  • Perception Cognition Action (PCA)
  • Use Related Risk Analysis (URRA) including (uFMEA)
  • Hazards & Hazardous Situations Analysis
  • Critical Task Identification
Helping you manage use related risk throughout the life cycle

TRAINING WORKSHOPS

Looking to empower students or team members in Human Centred Design or Human Factors Engineering? Our expert team has developed a series of interactive training workshops which incorporate engaging activities in:

  • Design Thinking & Human Centred Design in Healthcare
  • Human Factors Engineering in Medical Device Development
 

Each course can be customised to go as broad or deep in particular topics depending on your specific needs. 

Our workshops are suitable for students and businesses and we can deliver both in person and remotely.

Helping your team develop

HF REGULATORY DOCUMENTATION

We have an expert understanding of HF regulatory requirements for the USA, UK and EU including IEC62366, FDA HF guidance and MHRA HF guidance.

We provide support in preparing HF documentation from HFE plans, protocols and HFE reports for regulatory submissions.

Helping you meet regulatory expectations