فارما

Air and dust filtration is essential in pharmaceutical production to maintain cleanroom environments, ensure product purity, and protect both workers and the external environment. Pharmaceutical processes generate dust, aerosols, and fumes that can contaminate products or pose health risks. Effective filtration ensures that these contaminants are captured, supporting compliance with Good Manufacturing Practices (GMP) and regulatory standards.

Filtration in pharmaceutical plants typically involves pulse jet bag filters, cartridge filters, and enclosed dust extraction systems. These are used in areas where active ingredients and fine powders are handled, helping contain and collect airborne particles during material transfer, processing, and packaging. Filtration systems can also be integrated with isolators or enclosures for added containment in critical operations.

Filtration systems are a fundamental part of Good Manufacturing Practices (GMP) in pharmaceutical production. They ensure that airborne particles generated during production do not contaminate products, operators, or the environment. This helps manufacturers comply with guidelines set by regulatory bodies such as the FDA, WHO, and EMA, and ensures clean, safe, and auditable operations.