FAQs
What does THAY PHARMA do?
1
THAY PHARMA provides pharmaceutical human factors engineering services to help teams design, test, and validate safe, intuitive, and compliant products for real-world use.
What types of products do you support?
2
We support drug delivery devices, combination products, pharmaceutical software, digital health tools, and connected systems.
What services does THAY PHARMA offer?
3
Our services include user research, use prediction, user documents, and user testing, from early development through to summative validation.
Do you support regulatory submissions?
4
Yes. We help clients generate the human factors evidence needed to support regulatory expectations, including FDA, EU MDR, and related standards.
Do you design and test Instructions for Use?
5
Yes. We support the development, review, and validation of IFUs and other user-facing materials, including packaging, labelling, quick guides, e-IFUs, and digital content.
Do you run usability studies?
6
Yes. We conduct formative studies, summative studies, comparative studies, and human factors validation tests for pharmaceutical products.
Do you recruit participants for studies?
7
Yes. We recruit relevant participants for human factors studies, including patients and healthcare professionals, depending on the project.
Can you support international projects?
8
Yes. We have experience supporting projects across multiple countries and regulatory environments.
What experience does THAY PHARMA have?
9
THAY PHARMA has 12+ years of experience, 160+ completed projects, and 75+ global clients across healthcare.
How do I get started?
10
Contact us through the website to discuss your project and speak with a human factors consultant.