GMP regulations require:
Sterility testing is the last mandatory inspection process before product release.
The sterility check isolator will gradually replace the requirements that must have been implemented in a Class B background Class A environment.
The isolator adopts the ISOLATOR safety level, and the environmental control is at the A level. The large background environment can be applied to the D-class area or the CNC environment to ensure the release of the drug. And reduce the operating costs of the environment.
The aseptic transfer is integrated with the hydrogen peroxide sterilization and dye removal technology to achieve effective and rapid sterilization of the sample before operation and inspection, again reducing the risk.
The modular design, selection, loading and structure combination can be selected according to the customer inspection batch.
The operation adopts a sitting posture operation to reduce work fatigue and improve human accuracy.
It can meet the operation of toxic materials, and the system can realize the safe replacement function of the filter.
Suzhou headquarters：No. 99 Tongcheng Road, Weitang Town, Xiangcheng District, Suzhou
Contacts：Hu Ji Yong