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Minami

@Norie-Minami

Hello I am Minami the CEO of IT Support in Tokyo. US based COO of iSocialize and country manager of iSocialize, Japan.

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Health/Medical/Pharmaceuticals

TITAN Simulation

Our Vision and Approach TITAN Simulation is Twin Cities based, veteran owned, small business that delivers the highest quality, most realistic, medical education models ever created. We aim to reduce medical error with low cost models created in our image, for your knowledge. Our models are a display of the physiology of the patient. As an educator, you will never have to supplement your simulation with “the patient is now cool and clammy, and pale,” as our models do that. You have what you have is what we create. We have developed a thorough and efficient method for model development: Much like software, we use agile and scrum. We conduct translational science R&D in emulating tissues through Material Science, Engineering, and Art. This is where simulation sciences get real. We create patient specific functional anatomical models that are the display of the patient’s physical findings. These are simulators that look and feel like real people, representing the age, gender, BMI, ethnicity, and pathologies of all humans. Requirements development, gap analysis, educational needs analysis, Cognitive Task Analysis (CTA), latent error identification and planning al create knowledge of the educational environment, methods, and research platforms for outcomes based objective quantification of performance. We must catch up to the aviation industry and support the maturation and accountability of medical and patient education. Functional model development using Quality Functional Design (QFD) with clinically relevant metrics, fidelity analysis (tissue, anatomic, functional, affective), prototyping through commercialization, sales and distribution, and customer service / support. We support your Investigational New Device (IND) development with patient specific synthetic tissues that are manufactured with ISO 9001 / 13485 standards. This process creates known engineering constraints consistent for medical device verification up to phase IV of FDA approval without human trials.

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