Please contact me for subcontracting any of the following activities:
– Medical devices human factors engineering standards and guidances: user research, contextual inquiries, use FMEA, tasks analysis (PCA model), heuristic analysis, experts reviews with users, competitive analysis, user interface prototyping, usability testing (formative, summative), associated documentation, post-production updates, training, audits…
– Sustaining engineering: complex issues root cause analysis, corrections definition workshop, post-production risk management, legacy products clinical evaluation report update…
Company’s Keywords:
postproduction, root cause analysis, usability, investigation, medical devices, clinical evaluation, sustaining, risk management, user interface, human factors
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