REVOX® offers an efficient, organized sterilization operation, so you can be assured that your products are sterilized and processed to meet regulatory requirements and exceed your expectations. (Click on charts below for larger version.)
Our team of microbiologists provides expert Biological Indicators (BI) processing service. Our technical staff places BIs in the load for the sterilization cycle per validation protocol and process with your products. After products are sterilized, we will interpret BI results, and how it relates to your sterilization process. Once BI verification is complete, we provide sterilization cycle documentations with BI results, so you can determine the release date for your products.
Routine Sterilization Cycle Explanation
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Product Received |
Once your products are received, we promptly log them in our materials management system. This will ensure that your products are tracked throughout the time they are in our possession. |
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Product Staged |
Products are put in quarantine. Our technical staff will place BIs in the load for the sterilization cycle per validation protocol and process with your products. |
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Product Processed |
Products are placed in the sterilization chamber and are sterilized according to validation protocol. Cycle data are recorded and will be stored in our database. |
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Product Shipped |
Products are shipped according to your instructions as specified in the agreement. |
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Report Delivered |
We provide sterilization cycle documentations with BI results*, so you can determine the release date for your products. Depending on your product requirements, additional testing, such as bioburden, residual, endotoxin, and sterility validation testing, may be required. |
*Per FDA guidelines, contract sterilization facilities provide documentation of processing, not sterility claims. Customer is responsible to determine the sterility of the processed product.
