Eastern GMP Consulting, LLC is an independent pharmaceutical and biotechnology consultancy based in North Wales, Pennsylvania, USA. The firm supports drug developers across CMC, technical operations, and quality functions, with a service focus on CDMO/CMO/CPO/CRO vendor selection and management, CMC project and program management, process development and technology transfer for both small and large molecules, and validation of equipment, processes, and packaging. Additional areas include clinical and commercial packaging, serialization, supply chain management, post-launch technical services, and regulatory and quality compliance support. This is led by a principal with three decades of industry experience in technical operations, CMC project leadership, and senior process validation roles at large pharmaceutical organisations.