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Reusable Medical Device

In FDA, Microbiology, MRO by Ken Eddington

When a medical device manufacturer is preparing a reusable medical device for FDA submission they need to account for several items, including cleaning and disinfection validations. Performing these validations correctly …

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NAMSA Irvine Facility Expands

In Microbiology, MRO, News by Ken Eddington

NAMSA recently unveiled our newly renovated Irvine facility at an Open House.  With this renovation and associated expansion comes new test offerings including: shipping simulation, automated disinfection studies, and increased …