Latham BioPharm Group services

We offer comprehensive end-to-end process support for your CMC efforts–from early development and optimization endeavors, to progressing through scale-up during advanced development, to supporting your end commercial process. Consider us your trusted CMC partner throughout the entire process. Our consultants each have an average of more than 20 years of experience in the Pharma industry, from Development, Operations, Technical Services, Quality Assurance, Quality Control, Compliance, and Auditing. We provide expertise in formulation and design, process optimization, scale-up, technical transfer, CDMO selection/management, technical design, fill/finish, and protocol review, and our experience spans API, Drug Substance, and Drug Product activities.