We welcome healthcare industry members to benefit from our vast knowledge and experience, combined into one comprehensive technologically-oriented solution.
Our team excels at sterilization process development based on a product’s unique characteristics through cycle optimization.
By utilizing ethylene oxide, steam and vaporized hydrogen peroxide sterilization technologies, we aim to provide valid process design and to make available A-Z services, including development of a sterilization validation protocol, design and manufacture of Process Challenge Devices (PCDs), supply of biological indicators (BI), full execution of routine sterilization processes and reports generation.

Taryag Sterilization QMS complies with the requirements of ISO 13485:2016 and ISO 11135:2014 and is registered by the FDA.

Call us: ☎ +972-4-6776929
Email: ✉ [email protected]

Company’s Keywords:

packaging test, ethelyn oxide, cleaning, iso 11135, sterilization, clean room, fda, laser welding, peel, dye, sterility, iso 13485, incubation, iso, accelerated aging, bioburden, bubble, validation, test

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medical devices

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