APPLICATIONS
Industries we work with
The classification follows the product and the regulator, not the other way round.
What a room has to satisfy is set by the product, not by the industry name. A supplement plant and a pharmaceutical plant can run the same ISO class and still need different rooms, because one is answering to segregation and the other to a grade defined separately at rest and in operation.
Each page below sets out the class these facilities typically run at, the regulatory framework that applies in Malaysia, and what we supply into that kind of room.
Pharmaceutical · Grade A to D
A GMP cleanroom in Malaysia is graded A to D, and each grade has a different limit at rest and in operation.
Medical device · ISO 7 to ISO 8
A medical device cleanroom in Malaysia is usually ISO 7 or ISO 8, sized by the device class and how the product is finally sterilised.
Supplements and food · ISO 8
A halal cleanroom in Malaysia has a second layer of requirements on top of the classification, and segregation is the hard one to add later.
Laboratory · ISO 6 to ISO 8
A laboratory cleanroom in Malaysia often has to do two opposite things at once: keep the product clean and keep the sample contained.
Semiconductor and electronics · ISO 5 to ISO 8
A semiconductor cleanroom in Malaysia adds a requirement the regulated industries do not have: everything in the room has to handle static.