Planning for a clean room is much complex process, where all future uses and even the local conditions should also be considered. As the requirements of Cleanroom Testing And Certification differ from one company to another company, there are many different manufacturers that offer the modular systems and the components and even respond to the special requests.
What does clean room mean?
Clean rooms are generally used to create perfect atmosphere which is particle-free and necessary and hence it helps to keep the risk about contamination to be lowest. Like, for Cleanroom Certification, environment is perfectly basic condition for different applications. The Printed circuit boards, for instance, are stored and manufactured in clean rooms for avoiding the short circuits between tiny connections.
The Fume Hood Certification offers particle-free environment which is generally required in research and also in the pharmaceutical industry; where any such requirements for purity of air are well specified by the highly appropriate and crucial standards as per industry.
- Analysing the demand
Operating and Setting up a clean room is even the cost factor which should be properly calculated in every point while looking for the Clean Room Certifications. Apart from the cost of investment for a required technology, it even consists of expected cost of running. The clean room must always be dimensioned in proper way that it helps to meet the requirements and does never take up unnecessary space and resources. Because of the modular design, the clean rooms may also be extended as well as adapted to requirements with little or more effort. You need to bear this in your mind while you are planning for production and if it is expected to enhance in the near future.
- Defining requirements for clean room
According to the intended use, air in the clean rooms is well assigned to different kind of airborne particulate to the classes of cleanliness. The standard of DIN for Cleanroom Hepa Filter lists nine different classes where their distinguishing features are size and density of the particle density. In the food industry, the particle requirements are actually quite strict for processing as well as for the storage of the electronic components. Also, smallest particles may even lead to any kind of the serious defects. In pharmaceutical industry, guidelines of GMP apply, that consist of not just specifications for the density and size of the particle but also maximum load of the permission bacterial.
- Select the suitable system of ventilation
It depends specifically on requirements of respective ISO class about the ventilation system that is most appropriate for the clean room. In every such applications, air flow must be well designed to prevent deposition of the particles at such critical points and also to remove various particles as much as it is possible to outside. Certainly, all such accesses should also be kept free and must also be positioned in a way that they might not get adjusted in the daily operation. The units of Air conditioning are also available to control level of humidity and temperature in the clean room.