Vacuum Chamber Systems Guarantee Absolute
, Low Residual OxygenA line of vacuum chamber sealers has been specifically engineered to meet or exceed the
Multivac Inc., Kansas City, MO
www.multivac.com
validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its pre-determined specifications and quality attributes
Vacuum Chamber Systems Guarantee Absolute Validation, Low Residual Oxygen
A line of vacuum chamber sealers has been specifically engineered to meet or exceed the validation requirements of medical product manufacturers. Makers of sensitive medical products such as implantable devices, which require assurance of low residual oxygen inside the package, can deploy the C400 TC or C500 TC systems to guarantee results. Both models are built with solid seal bars, enabling a constant and verifiable temperature over the entire sealing surface throughout the full sealing cycle. The systems offer a validation package that is compliant with ISO 11607 standards. Additional features include precision parameter control and alarm capabilities, production data acquisition, visual and acoustic alarming, and external calibration and validation ports. Built from stainless steel and anodized aluminum, both models can be adapted to accommodate multiple product sizes.
Multivac Inc., Kansas City, MO
www.multivac.com
Pharmaceutical validation is a critical process that ensures that pharmaceutical products meet the desired quality standards and are safe fo...
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