“sterilization process”可以造什么句，sterilization process造句

The manufacturer shall subject the medical device to a validated sterilization process and record all the control parameters of the sterilization process.

Laparoscopic silicone rubber tube attachment of cap of medical instruments, laparoscopic in the high-temperature sterilization process, still can maintain good performance.

All the package materials shall be suitable for sterilization process. The inner package shall have excellent air-tightness and ensure the product free of Bacterium within its shelf life.

This guideline presents a pragmatic approach to the judicious selection and proper use of disinfection and sterilization processes;

The company shall establish documented procedure for the validation of sterilization process, which shall be earlier than the initial use.

Several novel disinfectant and sterilization processes are under development.

Since the earliest days of parenteral manufacturing it has been recognized that many drugs and biologics would not withstand a physical sterilization process in their final container.

The results of sterilization process validation shall be recorded together with the process data. Every year the sterilization process data shall require a re-validation.