Adragos Pharma is a contract development and manufacturing organization (CDMO) for pharmaceutical products. The company's core activity encompasses the development, manufacture and analysis of (bio)pharmaceutical products, including sterile and non-sterile liquids, semi-solids, tablets and suppositories. The company also offers services such as inspection, packaging, storage and distribution of pharmaceutical products.
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Aseptic manufacturing of (bio)pharmaceutical products
Aseptic manufacturing of sterile (bio)pharmaceutical products, either lyophilized or liquid, for small-scale clinical and commercial batches, at an EU-GMP certified site.
Clinical manufacturing
Clinical manufacturing Phase I, II and III, scale-up, technology transfer, pilot lots, GMP manufacturing, clinical packaging, GMP storage and shipment at controlled temperature.
Commercial manufacturing
Commercial manufacturing GMP, technology transfer, process validation, release testing, secondary packaging, serialization, GMP storage and commercial distribution.
Development services
Development of the lyophilisation cycle, development and transfer of the manufacturing process, support for formulation development, filter/material compatibility, specific developments on request.
Analytical services
Analytical services HPLC-UV, UPLC-UV, osmolality, pH, visible and sub-visible particles, sterility, endotoxins, biological load and contamination with specific germs.
Quality control
Control of raw materials and packaging items, in-process controls, sampling of finished product, release testing and stability studies according to GMP.
Primary and secondary packaging
Primary packaging defined by the customer according to the product specifications, visual inspection, manual or automatic labelling, secondary packaging.
GMP batch certification
GMP batch certification by Swissmedic for sterile lyophilised products and liquids, with GMP manufacturing of the first batches.
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