Accurate particle size segregation is critical for pharmaceutical formulations. Munit offers GMP-compliant sieving services to separate, classify, or deagglomerate powders — ensuring optimal flowability, blend homogeneity, and regulatory compliance.
Why Sieving Matters in Pharma
Sieving eliminates unwanted large particles, improves powder uniformity, and ensures that API and excipient blends meet defined particle size specifications. It’s particularly important in inhalation, oral solid dose, and sterile manufacturing.
Cleanroom Sieving Under GMP
All sieving is performed in cleanroom-classified areas, using pharma-grade vibrating or centrifugal sieves. Equipment is validated, calibrated, and cleaned per strict protocols, with full batch traceability.
Applications and Powder Types
We sieve:
- APIs after micronization
- Excipients before blending
- Sterile or low-dose compounds
- Cytotoxic or potent APIs (under containment)
Achieve uniformity with precision powder screening.
Discover Munit’s pharma-grade sieving services.