2021 Exhibitor List X Showroom

The approval process for ensuring the identity, potency, purity, safety and effectiveness of a biopharmaceutical is complex, but its effective navigation is critical to the product’s ultimate commercial success. With more than 50 years of experience, the Charles River Biologics Testing team has the proven knowledge, expertise and capacity to address challenging projects from biotechnology and pharmaceutical companies worldwide. We provide tailored global testing and manufacturing services to help accelerate drug development from concept to product release. Our primary emphasis is on quality, which is enforced through continual training and internal audit programs to ensure that our practices are in compliance with global regulatory guidelines. We support clients throughout the biologic development cycle, from discovery through preclinical and clinical studies to marketed product release. We have the capabilities to address the needs of clients based anywhere in the world and have specialized programs for companies that focus on vaccine, cell therapy and biosimilar development. Our facilities in the United States, United Kingdom, Ireland, France and Germany form a global scientific network, allowing us to provide our clients with flexible, comprehensive solutions to maximize resources and optimize results.