MEDICAL DEVICES — Thay Medical

The success in recruiting participants is due to participants (users) contacting us to be part of a study or test. By adhering to the current regulations surrounding ethical participant recruitment, we are able to safely bring people in to help in evaluating medical devices and pharmaceutical products in an industry-leading manner.

Participation in a Usability Study or a Human Factors Test gives you the opportunity to contribute to the development of successful and clinically accurate devices - be it an MRI Scanner or a new injection system or a diagnostic application! Without your involvement, pharmaceutical products, diagnostic systems and medical devices could be unsafe, create additional stress and harm and even bad user experiences. These are results we do not wish to ever see! Instead we like people of all types to be involved in the product development, to tell us what will work or not, to improve, to enhance and in the end, as a user, give yourself that positive user experience!

Planned Usability Studies and Human Factors Tests

The following Usability Studies and Human Factors Tests are currently being planned:

Are you an Interventional Cardiologist or a Radiological Technologist?

Study / Test: Human Factors Validation Test on an OCT Imaging System.

Purpose: To prove that an innovative Imaging System is safe and effective in use.

Location of Study / Test: Chicago, Illinois, USA.

Planned Dates of Study / Test: November 2025.

Participants required for the Study / Test: User Group 1: Interventional Cardiologists

User Group 2: Radiological Technologists

User Group 3: N/A

Time required for an individual Study / Test session(s): User Group 1: 2.5 hours

User Group 2: 3.5 hours.

User Group 3: N/A

Incentive offered for this time: Please contact us.

Are you a Tissue Viability Nurse, a persons diagnosed with Diabetes or a Caregiver of a diabetic patient?

Study / Test: Human Factors Pre-Validation Test on a Wound Dressing System.

Purpose: To prove that an innovative Wound-care System is safe and effective in use.

Location of Study / Test: San Antonio, Texas, USA.

Planned Dates of Study / Test: December 2025.

Participants required for the Study / Test: User Group 1: Tissue Viability Nurses, Ward Nurses, Diabetes Specialists

User Group 2: Diabetic patients

User Group 3: Caregivers of diabetic patients

Time required for an individual Study / Test session(s): User Group 1: 2.5 hours

User Group 2: 2.5 hours

User Group 3: 2.5 hours

Incentive offered for this time: Please contact us.

Are you a user of facial dermal fillers?

Study / Test: Readability Test on an Instructions for Use for a facial dermal filler.

Purpose: To prove that an Instructions for Use and supporting user documents are readable.

Location of Study / Test: Online, UK.

Planned Dates of Study / Test: December 2025.

Participants required for the Study / Test: User Group 1: Lay users of facial dermal fillers

User Group 2: N/A

User Group 3: N/A

Time required for an individual Study / Test session(s): User Group 1: 1.0 hours

User Group 2: N/A

User Group 3: N/A

Incentive offered for this time: Please contact us.

Contacting us to participate in a study / test is easy!

If you would like to find out more about participating and being paid to be part of a Usability Study or Human Factors Test, please enquire below.

Enquire about participation

OUR UK OFFICE

Unit 2, Hawthorn Farm Business Park, Winterborne Stickland,

Blandford Forum, Dorset, DT11 0NB, ENGLAND.

+44 (0) 1258 881600

enquiries@thaymedical.com

REGISTERED IN ENGLAND COMPANY NUMBER 9211177

QUICK LINKS TO OUR SERVICES & EXPERTISE

Total Compliance™

[]

Human Factors Intelligence™

[]

Medical Device (MDR/CE) Usability Compliance

Use Error Prediction™

US FDA Human Factors Compliance

Remediation Usability Testing

Summative Usability Studies

Formative Usability Studies

Human Factors Validation Tests

SITE MAP

HOME

SOLUTIONS

PHARMACEUTICALS

ABOUT US

NEWS & INSIGHTS

MEDICAL DEVICES

PARTICIPANT RECRUITMENT

CONTACT US