CMAB strives to achieve a culture of continual improvement and customer focus with product quality, safety and efficacy as the expected outcome. Therefore, CMAB developed our Quality System to comply with the applicable laws, rules, regulations, standards and guidance associated with pharmaceutical Good Manufacturing Practices (GMP) standards, including but not limited to China Food & Drug Administration, US Food & Drug Administration (21 CFR), European Medicines Agency (Eudralex), WHO, and PIC/S and ICH standards.
Built to provide high-quality CDMO services from the ground up, CMAB has adopted leading information technology products to streamline operations and assure delivery from our inception. Key platforms include：
• Laboratory Information Management System (LIMS)
• Enterprise Quality Management System (EQMS)
• Enterprise Resource Management System (ERP)