We specialize in aseptic manufacturing of lyophilized or liquid sterile (bio)pharmaceutical drug products through fill and finish.

We specialize in the aseptic production of lyophilized or liquid sterile (bio)pharmaceutical products through fill and finish. Our facility is ideal for the production of small clinical and commercial batches and is GMP and FDA certified.
Clinical Manufacturing – Phase I, II, & III
Commercial Manufacturing – Fill and Finish
We are specialized in two distinct dosage forms: liquid products aseptically filled and lyophilized products, both filled in vials. Capacities: Aseptic Filling, Liquid Filling, Complex Formulation, Peptides, Biological Products, Controlled Substances, Small Molecules, Sterile Suspensions, Ophthalmic Products, Placebos/Diluents, Vials, Lyophilizer Size (3.5 m²).
No minimum batch size is imposed. Specialized in the manufacturing of clinical batches from very small quantities of bulk solution (eg: 200-300ml).
We manufacture batches for the different phases of pharmaceutical development, from manufacturing under GMP and FDA conditions (first stage of scale-up under industrial conditions, preparation of material for preclinical studies, stability studies, etc.) to GMP/FDA manufacturing for clinical needs.
Development Services
Freeze-Drying Cycle Development
Manufacturing Process Development and Transfer
Formulation Development Support
Filter/Material Compatibility
Analytical Services
Primary & Secondary Packaging
Quality Control
GMP Batch Certification