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A company has decided to globally market a product that is intended to disinfect medical device. Which should be considered FIRST when registering this product

A company has decided to globally market a product that is intended to disinfect medical device. Which should be considered FIRST when registering this product as a medical device?

a.Product stability and shelf life

b.CompanyQMS and technical documentation

c.Classification of the product

d.Reprocessing validation requirements

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