The aseptic filling production of biological agents must be carried out in the environment of Class100 (ISO5,Class A). According to different background environment, the local environment of filling machine can be divided into LAF (Laminar Airflow), RABS(Restricted Access Barrier System, Open or closes) and isolator.
ORABS is an open restricted access barrier system, which is the most commonly used filling barrier at present. It is equipped with a glass door metal frame and intervention gloves, and a static pressure box to provide one-way vertical air flow at top, and supply air at top is discharged from the bottom and returned through B-class background.
Figure 2: ORABS
With the increasing maturity of Isolator technology and increased risk awareness of production staff, the isolator has been widely used in a C-class or D-class clean area. All personnel operation and material / tool transfer during production can not destroy tightness of the system. The isolator should be automatically cleaned with VHP before use, and its repeatability and controllability need to be verified.
Figure: Isolator
The aseptic filling production of biological agents must be carried out in the environment of Class100 (ISO5,Class A). According to different background environment, the local environment of filling machine can be divided into LAF (Laminar Airflow), RABS(Restricted Access Barrier System, Open or closes) and isolator.
ORABS is an open restricted access barrier system, which is the most commonly used filling barrier at present. It is equipped with a glass door metal frame and intervention gloves, and a static pressure box to provide one-way vertical air flow at top, and supply air at top is discharged from the bottom and returned through B-class background.
With the increasing maturity of Isolator technology and increased risk awareness of production staff, the isolator has been widely used in a C-class or D-class clean area. All personnel operation and material / tool transfer during production can not destroy tightness of the system. The isolator should be automatically cleaned with VHP before use, and its repeatability and controllability need to be verified.
The aseptic filling production of biological agents must be carried out in the environment of Class100 (ISO5,Class A). According to different background environment, the local environment of filling machine can be divided into LAF (Laminar Airflow), RABS(Restricted Access Barrier System, Open or closes) and isolator.
ORABS is an open restricted access barrier system, which is the most commonly used filling barrier at present. It is equipped with a glass door metal frame and intervention gloves, and a static pressure box to provide one-way vertical air flow at top, and supply air at top is discharged from the bottom and returned through B-class background.
With the increasing maturity of Isolator technology and increased risk awareness of production staff, the isolator has been widely used in a C-class or D-class clean area. All personnel operation and material / tool transfer during production can not destroy tightness of the system. The isolator should be automatically cleaned with VHP before use, and its repeatability and controllability need to be verified.
The aseptic filling production of biological agents must be carried out in the environment of Class100 (ISO5,Class A). According to different background environment, the local environment of filling machine can be divided into LAF (Laminar Airflow), RABS(Restricted Access Barrier System, Open or closes) and isolator.
ORABS is an open restricted access barrier system, which is the most commonly used filling barrier at present. It is equipped with a glass door metal frame and intervention gloves, and a static pressure box to provide one-way vertical air flow at top, and supply air at top is discharged from the bottom and returned through B-class background.
With the increasing maturity of Isolator technology and increased risk awareness of production staff, the isolator has been widely used in a C-class or D-class clean area. All personnel operation and material / tool transfer during production can not destroy tightness of the system. The isolator should be automatically cleaned with VHP before use, and its repeatability and controllability need to be verified.