Engineered for GMP Production
DIAGNOSEX process lines are designed for a broad range of pharmaceutical products — including sterile injectables, lyophilized formulations, vaccines, blood products and IVD reagents. Each station shares electrical, control and data standards — reducing integration time and qualification effort for CDMOs and manufacturers.
Industrial-scale DAC columns for synthetic, peptide, oligonucleotide and small-molecule API purification with full IQ/OQ.
Aseptic micro-dosing of liquid formulations, 25 μL – 10 mL range with single-use tubing to prevent cross-contamination.
Sorting, filling, stoppering under LAF, GMP-oriented design with SUS 316L contact parts.
In-situ pre-freeze, primary drying and hydraulic stoppering under vacuum, recipe-based PLC control.
Aluminum cap crimping for hermetic, sterile final container closure under cGMP conditions.
Decades of Experience. One Reliable Partner.
From small-molecule APIs to advanced biologics — DIAGNOSEX equipment supports the full spectrum of pharmaceutical and biopharmaceutical manufacturing.
Peptide API purification and lyophilized formulation for GLP-1 analogs and custom peptides.
Recombinant insulin purification, sterile filling and freeze-dried powder production.
Lyophilized and liquid vaccine formulation, aseptic vial filling and sealing.
Powder-for-injection production with sterile filling and crimp sealing.
Plasma fractionation, coagulation factors and albumin lyophilization.
IVD lyophilized beads, magnetic bead liquids and micro-dosing reagents.
siRNA, ASO and mRNA lipid nanoparticle formulation and aseptic filling.
Collagen, hyaluronic acid and peptide-based cosmetic lyophilized formulations.
Every DIAGNOSEX system ships with full validation documentation to accelerate your facility qualification timeline.
All equipment is designed and manufactured in accordance with EU GMP Annex 1 and FDA cGMP guidelines for sterile medicinal products.
Comprehensive qualification packages delivered with every system, with full traceability and on-site support.
Built-in process analytical technology and data integrity features ensure reproducible, auditable batch outcomes.
Get a customized equipment proposal tailored to your product, batch size and regulatory requirements — typically within 3 business days.
