As the medical industry continues to evolve and become increasingly user-centric, research methodologies such as Contextual Inquiry (CI) have garnered interest from medical device professionals. However, many interested human factors (HF) practitioners and medical device manufacturers are inexperienced with CI and may benefit from experience-based guidance beyond that found in industry standards (e.g. FDA Guidance, AAMI, etc.).
This poster shall summarize CI best practices drawn from BlackHägen’s unique experience with carrying out CI endeavors around the world.
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