Cellectar has planned for a structured and documented management system with the procedures, organizational authority, responsibilities, and accountability that will facilitate GMP manufacturing throughout the life of the company.
Cellectar has also engaged quality consultants to provide the expertise and extra hands needed to develop the procedures for the validation and operation of the manufacturing equipment and the plant in general. An electronic document management system was chosen as the cornerstone of the quality system, functioning as a dynamic database that will store, maintain, and track all documentation, including pre-clinical and clinical documents.
