Ví dụ về việc sử dụng The sterilization process trong Tiếng anh và bản dịch của chúng sang Tiếng việt
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This is where the sterilization process begins.
You shouldn't have too many in a bag because it might hinder the sterilization process.
The sterilization process will not start until the chamber is at the right temperature.
This applies in particular to the sterilization processes.
The sterilization processes, sterilizer capacity and the design match the corresponding sterilization goods.
Thanks to the plasma generation, the by-products of the sterilization process are water and oxygen.
Just like with autoclaving,the medical tools are placed into bags during the sterilization process.
The sterilization process manipulates the value of a domestic currency relative to another, it's initiated in the foreign exchange market.
However, some manufacturing situations require a modified orspecialty Biological Indicator to assist in validating the sterilization process.
Door interlock switchensures the automatic closure of cabinet door after the sterilization process starts(under this condition, the door cannot be opened manually).
And when the temperature inside retort reaches the programmed sterilization temperature,it will be kept during the sterilization process.
The sterilization process used to destroy or remove microorganisms is probably the single most important process in the manufacture of parenteral FPPs.
Finally the cooling water through heat exchanger willcontinually make those sterilization water cool down until the sterilization process is finished.
However, for sterile APIs, full validation data on the sterilization process should be provided in the Open part(in cases where there is no further sterilization of the final product).
If the liquid needs to be filled with hot filling(liquid filling temperature is higher than 70° C), usually the temperature is higher than 70° C,you don't need to set up the sterilization process, where most bacteria have been eliminated.
After one sterilization cycle, it can determined that the sterilization process fulfills the eligible requirements when the indicator color patch becomes standard color or darker from original yellow;
Description, documentation, and results of the validation and/or evaluation studies should be provided for critical steps orcritical assays used in the manufacturing process(e.g. validation of the sterilization process or aseptic processing or filling).
The sterilization process should be described in detail and evidence should be provided to confirm that it will produce a sterile product with a high degree of reliability and that the physical and chemical properties as well as the safety of the FPP will not be affected.
If the sterility of the FPP is based upon the sterile manufacture of the API then data on the sterilization process together with full validation data should be provided.
The in-situ sterilization process is similar to the process of scale-up experiments.
The whole sterilization process is completed inside the EUT Unit.
After the preconditioning stage, the long and complicated sterilization process starts.
Easy-seal flap to ensure the integrity of contents after sterilization process.
The whole sterilization process is under PLC automatic computer control and temperature difference +0.3°C in the retort.
The whole sterilization process is under PLC automatic computer control and temperature difference +0.3°C in the retort.
PTFE or PFA liner for hygienic purpose or high-temperature sterilization process.