MEDICINE

In the pharmaceutical industry, air filtration is of critical importance to maintain product quality and minimize the risk of contamination during the production process. Air filters are used in pharmaceutical manufacturing facilities, laboratories, sterilization rooms and storage areas. The use of air filters in these areas is critical to maintaining the quality of medicines, reducing the risk of contamination and ensuring the safe production of products.

 

Filter Selection Criteria for the Pharmaceutical Industry

 

Among them: There are several critical points to consider when choosing filters in air conditioning systems for the pharmaceutical industry.

Compliance with Air Quality Standards: Air quality is extremely important in pharmaceutical production facilities. Therefore, filters must comply with international air quality standards (such as ISO 14644-1).
Particle Capacity: It is very important that the particles generated during drug production are efficiently retained by the filter. Therefore, when choosing a filter, care should be taken to ensure that the particle capacity is sufficient.
Disinfection Features: Filters used for the pharmaceutical industry must have disinfection features. Especially when production is carried out in sterile environments, filters must effectively prevent microbes and other harmful organisms.

 

Filter selection made by paying attention to these criteria plays a critical role in providing a clean and reliable production environment for the pharmaceutical industry.

 

NAF Filter, which will meet the need for clean air and all requirements in the pharmaceutical industry, offers the most appropriate solutions.

Classification for Clean Rooms in the Pharmaceutical Industry

 

Areas where the drug is produced; It must ensure perfect compliance with the "Good Manufacturing Techniques (GMP)" requirements for general pharmaceutical production techniques.

 

Class A: Regions requiring the highest degree of sterility; for example, aseptic zones with open filling. Air must be pumped into these areas in a laminar manner at 0.45 m/s +/- 20%.
Class B: Sterile areas surrounding the Class A site.
Classes C and D: Less critical clean areas, such as equipment washing, solution preparation areas.

PHARMACEUTICAL INDUSTRY APPLICATIONS

PHARMACEUTICAL PRODUCTION AREAS

CLEAN ROOM

LAB

STORAGE