At Improvita, we uncover critical user insights to support the design, development, and validation of medical devices, combination drug devices, and AI enhanced software as a medical device (SaMD). 
 
Key services include:

Human Factors Validation & Formative Research
Usability Testing for Devices, Diagnostics, and Digital Tools
Patient-Centered Design for SaMD and Combination Products
FDA & Notified Body-Compliant HF Studies
Behavioral Science Applied to MedTech UX
UX Research for Risk-Based Design Decisions
HCP and Patient Engagement in Product Design
Ethnographic and Contextual Inquiry in Healthcare Settings

Conducting comprehensive Human Factors/Usability and User Experience studies early and throughout the development process can provide essential data necessary for FDA regulatory approval upon the first submission.

The goal of the Improvita team is to optimize the user experience; let's make it easy for the user to use your product easy to use safely and efficaciously!

Improvita

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