Active Pharmaceutical Ingredients (API)
Filtration plays a critical role in API production, where crystallization, catalyst removal, and purification steps demand high solids capture and product purity. DrM filtration systems provide closed, automated separation of fine crystals, catalyst residues, or intermediates under GMP-compliant conditions. Their ability to integrate cake washing, drying, and enclosed discharge supports process efficiency while minimizing product loss, contamination risk, and operator exposure. These systems are scalable for both clinical batch production and large-scale manufacturing environments.