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The license allows for GMP bulk drug substance manufacturing to support all phases of clinical studies.
April 18, 2023
By: Anthony Vecchione
Sterling Pharma Solutions, a global contract development and manufacturing organization (CDMO), has been granted a Manufacturer’s Authorization for Investigational Medicinal Products from the UK’s Medicines and Healthcare products Regulatory Agency (MHRA). The license allows Sterling to manufacture antibody-drug conjugates (ADCs) for clinical use in its current good manufacturing practices (cGMP) compliant manufacturing facility in Deeside, UK. Sterling acquired the 6,500 square-meter-s...
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