Quality Assurance
Our Quality Assurance teams are focused on ensuring that quality is the core principle of everyday operations at Cambridge Major. Quality Assurance ensures that every stage of the manufacturing process (receiving of Raw materials, release of Intermediates and Active Pharmaceutical Ingredients, testing and packaging) meets all customer and regulatory expectations, whether the product is going into the US or European markets. This is achieved through our focus on quality and materials management, documentation and records, laboratory controls, and comprehensive SOPs. Our Quality Assurance teams work closely with clients to facilitate site audits and manage any GMP issues that arise during the manufacturing process. Furthermore, CML’s Quality Assurance unit supports the process flow through all phases of drug development and through validation and commercialization efforts.
Cambridge Major Laboratories welcomes you to visit our facilities in North America and Europe to see for yourself our commitment to Quality. |
