During clinical stage development, quality supervision guarantees that the fundamentals of Good Manufacturing Practices (GMPs ) are consistently applied. Quality is built into the different phases of clinical development to secure:
The safety and rights of our studies’ participants
The reliability of the data submitted to health authorities
The complete adherence to all current Good Clinical Practices (GCPs)
Our clinical Quality Management System encompasses clinical research documents, activities and information management systems. Moreover, Teva ensures that quality is a main concern not only in our own processes and procedures, but also in those of our vendors, investigators, contractors who collaborate with us at the clinical stage.