Medical Device Human Factors Validation Specialists
Proving your medical device is safe, intuitive and satisfying to use before launch.
ISO 13485 certified ● 12 years operating globally
Expertise across
Medical Devices
Summative Usability Studies
Human Factors Validation Tests
Pharma Devices
Comparative Use HF Studies
Readability Studies
Artificial Intelligence
AI-Driven Software Tests
Worst Case Usability Studies
In Vitro Diagnostics
Actual Use Validation Tests
Self-selection Studies
Validation services for your device development:
Human Factors Validation Tests
Summative Usability Studies
Readability Studies
Self-selection Studies
Comparative Use Human Factors Studies
AI-driven Software Testing
Human Factors support beyond testing
MEDICAL DEVICE HUMAN FACTORS PLANNING
Planning your Human Factors Validation activities for single and multiple regulatory submissions is something we love to help you determine.
MEDICAL DEVICE HUMAN FACTORS ENGINEERING
Taking over from early stage and concept device development to complete the Human Factors Engineering process for compliance and user performance.
USING AI IN HUMAN FACTORS ENGINEERING
Reducing the time for verification and validation activities through the use of AI tools, predictive data and our expert-led experience.
THAY Medical at a glance
100%
Participant recruitment in our studies and tests globally
180+
Projects completed over the past twelve years
100+
Validation Tests, Readability, Comparative Use and Summative Usability Studies completed globally
12 years
Using our ISO 13485 certified Quality Management System
Our valued customers
Have An Enquiry? Or simply want to find out more…
Talk to THAY Medical about Human Factors support for your project
+44 (0)1258 881600
