Pharmaceuticals
GMP sieving with documentation to match
Pharma lines demand more than particle separation: they demand validation. Every VortiSep pharma-build machine ships with material certificates (3.1B), surface-finish maps, IQ/OQ documentation support and crevice-free electropolished contact surfaces — sized for rooms, not just processes.
Typical working context · PharmaceuticalsWhat runs through the mesh
Your material not listed? That is what the sample test is for — send it and it goes on file with numbers.
What keeps pharmaceuticals engineers calling
Cross-contamination control
Single-deck, fully-draining designs with validated cleaning protocols between product changeovers.
Electstatic API blinding
Ultrasonic systems at 33 kHz keep low-density API powders flowing through 200–400 mesh.
Containment of potent compounds
Glove-box interfaces, continuous liners and dust-tight transfer keep OEL limits respected.
Audit trail expectations
Equipment documentation package delivered with the machine — serials, weld logs, finish readings.
What we would install — and why
Build options this industry orders
Design targets and documentation expectations the machines are configured against.
- cGMP design
- GMP documentation pack
- Ra ≤ 0.4 μm electropolish
- ATEX option
Case studies in this industry
Pre-packing scalping at 5.2 t/h — zero filler stoppages in 14 months
Remove tramp oversize before the filler without reducing the 5 t/h packing rate.
325-mesh zinc powder cut held at 800 kg/h with ultrasonic deblinding
Hold a continuous −325 mesh guard cut at ≥ 800 kg/h with shift-length mesh intervals.
Screening pharmaceuticals materials — before you buy
Describe the material and the cut. The reply states the recommended series, its limits for your case, and what a sample test would add.