Pass Box Cleanroom Furniture for Pharmaceutical Industry in Building Material Shops

Introduction to Cleanroom Pass Boxes

Pass boxes are a component of a cleanroom system that allows for transfer of items between two areas of differing cleanliness. These two areas can be two separate cleanrooms or a non-clean area and a cleanroom. Utilizing pass boxes decreases the amount of traffic in and out of the cleanroom, which saves energy and lowers risk of contamination. Pass boxes are often seen in sterile laboratories, electronics manufacturing, hospitals, pharmaceutical manufacturing facilities, food and beverage production facilities, and many other clean manufacturing and research environments.

What is a "DOP" Pass Box?

DOP Pass boxes are equipped with leak and pressure detection technology required by new GMP Standards.

 
With our DOP Pass Boxes you can be assured of your HEPA filter integrity and pass box internal pressure at all times.

E-Clean Pass Box Advantages

(1) Durable

Our pass box exteriors are constructed of SUS304 Stainless Steel or high-quality steel plate, while our interior surfaces are 100% Stainless Steel. 

(2) Modern

We use top of the line E-Clean HEPA Filters in our pass boxes to ensure that unwanted particles are filtered out of the environment. High powered UV lights also ensure that the pass box is kept free of contaminants.

(3) Safe

Available magnetic and electronic locks prevent both pass box doors from opening at the same time, which in turn prevents contaminaion of the clean area by air from the less clean area. 

(4) Flexible

We manufacture DOP, Air Shower Style, and Traditional Pass Box models to fit your needs. We offer six standard sizes, and can produce any size with custom dimensions according to customer requests.

Pass Box Usage Procedures

Pass boxes should be designed to meet the cleanliness level of the cleaner of the two areas that they connect. For example, if a pass box connects a printing room (FS209E 100,000 / ISO 8) and a packaging room (FS209E 10,000 / ISO 6) at a pharmaceutical plant, the pass box should meet 10,000-level (ISO 6) standards. Furthermore, personnel from the clean area should be responsible for cleaning the pass box and sterilizing it with the UV light for 30 minutes per day at the end of the shift.

(1)   The channels for goods and personnel to enter/exit the cleanroom should be clearly separated--both physically and with an adequate amount of signs indicating the purpose of each passage.

(2)  When using a cleanroom pass box, personnel must strictly adhere to the "one door at a time" rule. That is, both doors cannot be open at the same time in order to avoid cleanroom contamination. Only when the door on the opposite side has been sealed can the door on the other side be opened.

(3)  When items leave the cleanroom via the pass box, they should be moved to their next process destination or to a buffer area in a timely fashion.

(4)  Any waste or potential contaminants should have a dedicated channel by which they should be transported out of the clean area.

(5)  Remember to regularly clean and sanitize your pass box and related areas on a regular basis

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