Telephone:  01767 600 886


Our Policy's


Medical/ Healthcare


Human Factors and the Usability Engineering File

Learn how to create all UE file documents in-line with the expectations from IEC62366-1 and the FDA.


This includes how to write a Use Specification, User Interface Evaluation Plan, Use Risk Analysis (Overview), User Interface Specification, Formative Evaluation (Overview), Summative Evaluation (Overview) and HFE Summary Report.

Planning and executing Human Factors Formative and Summative studies
Learn all there is to know about how to Plan, Prepare, Execute and Report Formative and Summative Evaluations and they key differences between both approaches.


This includes how to write protocols, discussion guides, moderate studies (Overview) and write fully regulatory compliant reports for the European and US markets

Usability testing Accompanying Documentation 


Learn how to plan, design and evaluate Instructions for Use, Training documentation, Labelling and Packaging.

This includes essential guidance for creating these types of materials, how to test comprehension and ask knowledge based questions.

1 Day Course

1 Day Course

1 Day Course

How to Moderate Formative and Summative studies 


Learn how to become a Moderator for Usability studies, Formative evaluations and Summative Evaluations.

This course will cover key steps to help ensure your Moderation technique allows rich data to be extracted in a meaningful un-biased way.

Human Centred Design, UX and UI principles (How to host a 5 day UX sprint)


Learn how to host a Human Centered Design/ User Experience Sprint in as little as 5 days!

This action packed course takes an initial high-level goal and turns it into a user tested concept within 5 steps. The course covers up to 25 methods.

Human Factors and Design


Learn how to use Co-Creation techniques to elicit insights from end users which cannot be gained through direct questioning methods.

Co-creation is a technique which involves end users designing their ultimate product to understand deeper (un-met) user needs which cannot be verbalised.


Co-creation can help ignite creative design brainstorms and radicalise design thinking. 

Maximising Qualitative and Quantitative Human Factors Approaches within User Research


Learn more about Qualitative and Quantitative Research and when to use each method to gain the best outcomes.

Understand how Qualitative and Quantitative Research compliment one another and how to analyse the data gathered from both approaches.

2 Day Course

1 Day Course

1 Day Course

1 Day course


£395 (+ VAT)

*2 Day course


£695 (+ VAT)

* 2 Day courses: Discounted cost applies when booking Two 1 Day courses on the same booking.
10% Early bird discount for bookings made up to 2 months before the event.
15% discount for 3 or more delegates on the same booking.



Quotes for custom training courses can be obtained by email. Please get in touch by emailing or by calling us on +441767600886 or +447905796532.


Course: Human Factors and the Usabilty Engineering File

7th November 2017 in London, United Kingdom

Course: Planning and Executing Human Factors Formative and Summative Studies

14th November 2017 in London, United Kingdom

Course: Human Centred Design, UX and UI principles (How to host a 5 day UX sprint)

21st - 22nd November 2017 in London, United Kingdom

Course: Use Risk Management for Medical Devices

29th November 2017 in London, United Kingdom

Course: How to Moderate Formative and Summative Studies

5th - 6th December 2017 in London, United Kingdom

Note: All prices include Lunch and Refreshments each day.


At the Human Factors Centre we ensure our courses are suited to each of our individual delegates needs to ensure that effective learning and knowledge transfer can be best utilised.

Our courses are designed to be taken by a range of individuals who work in roles that directly interface with end users.


This includes (but is not limited to):

  • Human Factors Engineers

  • User Experience Designers

  • Researchers

  • Product Designers

  • Mechanical Engineers

  • Software developers

  • Product Managers

  • Product Owners

  • Development Teams

  • Regulatory

  • Risk Management teams

  • Safety Engineers

  • Clinical product specialists

  • Clinicians advising on Human Factors

  • Clinical Trial Managers

  • Project Managers

  • Quality Assurance Managers

Can't make one of these dates, course not currently listed or need training sooner? Contact us to arrange an in-house training programme and we would be happy to conduct a course at your company. Please note prices may vary depending on location and the number of delegates taking part.

2 Day Course

Use Risk Management for Medical Devices


Learn how to conduct a comprehensive Task Analysis and Perception, Cognition and Action (PCA) analysis on a product.


Learn how to feed these analyses into a Use Failure Modes and Effects Analysis (uFMEA) and how to identify Critical Tasks from the output.


Learn how to create User Interface Requirements and how to manage this throughout a projects lifecycle.

1 Day Course

To book onto one of our courses, please fill out your details in the registration form below and let us know which course you are interested in!

If you are interested in any of the courses listed above please get in contact and check availability or register for a course!

Don't forget!

To tailor our training to suit your needs, we also offer a range of 1-3 day customised training programmes where we take your training requirements and build a customised training programme made just for you. If you are interested, let us know and we will arrange a call or come in and see you!