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QUAY Pharma is experienced in the formulation development of live biotherapeutics and is one of the few companies licensed for the clinical manufacture of the finished dosage form of live biotherapeutics. Quay has a lot experience in the understanding of the client dosing requirements for the live bio therapeutic. Quay can prepare a formulation development strategy to bring it rapidly and effectively to First in Man (FIM) studies and on to further clinical use aiming to provide a formulation with the best clinical outcome. Quay is experienced in working with single strains and consortia products from our GMP, MHRA and FDA inspected facilities.