LABORATOIRES KABS INC.

Since 1997, KABS has offered a broad range of advanced pharmaceutical product development services to the pharmaceutical industry worldwide. Our team of more than 150 specialists support development programs from initial discovery to phase III and commercialization. KABS supports drug developers from early stages to commercial manufacturing. Our Integrated CDMO services include formulation development, stability studies, method development, manufacturing of pre-clinical to late-stage clinical trial prototypes, scale-up, registration batches and manufacturing of approved drugs. We perform aseptic manufacturing of liquid or lyophilized parenteral drugs in batch sizes from 100 to 100,000 vials. KABS provides spray drying services and solutions. KABS promotes analytical continuity in testing impurity profiles of new drug substances and corresponding new drug products. KABS is a WHO prequalified Quality Control Laboratory. We perform quantification of elements in drug substances and excipients and primary packaging. KABS pharmaceutical proficiency testing programme is recognised as a demonstration of laboratory quality and competency by a range of third parties.