Pace® Life Sciences provides a full suite of contract CMC development, clinical trial materials manufacturing, GMP analytical testing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries. Our network of CDMO sites consists of premier research and development facilities, GMP analytical testing laboratories, and manufacturing support service centers. Our experienced, highly trained industry experts and our investment in state-of-the-art development and manufacturing facilities emphasize our commitment to efficiently advancing client programs through the clinic to commercialization. We are dedicated to delivering the best and most reliable services with positive customer experiences across all channels of our business.

Our services continue to expand into novel therapies, including medical devices, combination products, antibody-drug conjugates, and lipid nanoparticles. We take pride in offering a wide range of services and innovative technologies while maintaining devoted relationships with our customers. Partnering with Pace means accessing a vast set of skills to support various aspects of your program, such as regulatory affairs consulting to explore alternative submission pathways.