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LAF - Laminar Air Flow
It is a dynamic barrier of HEPA-filtered unidirectional air flow to move particles away from the filling/closing area.
The line must operate in a clean room grade B or higher.
Due to the growing concern for product and operator protection and the complex regulatory framework of the pharmaceutical industry, it became essential to design the processing equipment together with the containment system.
Aseptic pharmaceutical manufacturing requires the production area to be free from microbiological and particle contamination. The environmental conditions for sterile processing are designed to maintain product sterility and are ISO 5 or Grade A classified, considering the following parameters:
In accordance with these standards, Dara Pharma has developed a wide range of products for different environmental conditions.
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