About The Author
Cleanroom door for GMP pharmaceutical
The cleanroom door is different from ordinary home doors. It is beyond the reach of ordinary home doors in terms of performance, accessories, and manufacturing technology. Because of its superb and complicated cleanroom environment, many customers have a headache in purchasing cleanroom doors.
Requirements for cleanroom doors
Choosing the correct door system is a major factor in ensuring the delicate balance of a cleanroom. If the doors do not function properly, the cleanroom could fail to meet relevant cleanroom standards and be exposed to a higher risk of contamination. Here are some of the most basic but essential factors to consider when selecting a cleanroom door.
Cleanroom Doors Make The Difference
Whether it’s a Class 100 or a Class 10,000 cleanroom, manufacturers in pharmaceutical, biopharmaceutical, medical device, electronic, and other critical manufacturing industries require their cleanrooms to be simultaneously functional, flexible, economical, practical, and of course, clean. But, while the current ISO 14644-1 and ISO 14644-2 Standards still call attention to the function of air filtration and air distribution in cleanroom design, the regularity and relative consistency of these systems across manufacturing platforms has ushered in a new age of cleanroom design focused on all components of the room, including floors, walls and especially doors.
The selection of cleanroom flooring
Cleanroom flooring systems must take account of the whole production process and materials must be chosen that will not give rise to airborne molecular or particle contamination. At the same time they must withstand harsh cleaning regimes and strong cleaning agents and disinfectants





