Human-Centered Healthcare Research

We support pharmaceutical and medical device companies with readability testing, human factors research, and evidence-based product development.

  • PIL Readability

    We conduct Patient Information Leaflet (PIL) readability testing and bridging assessments for EU regulatory submissions. Our studies evaluate how patients find, understand and use medicine information, providing documented evidence to support regulatory requirements.

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  • Human Factors

    We evaluate medical device usability, including the product, instructions, packaging and labelling. Through formative and summative studies, we identify usability issues, use errors and potential risks, supporting safe and effective use in accordance with IEC 62366-1.

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  • Product Design

    We support healthcare product development through user research, concept evaluation and usability testing. By understanding user needs, behaviours and real-world challenges, we help teams validate assumptions and make evidence-based decisions throughout the design process.

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Why Cognitiva?

We combine hands-on research experience with an understanding of pharmaceutical and medical device requirements. From study design to reporting, we focus on clear evidence and actionable findings.