Lloyd’s Register Serentec, Inc., a leading provider of validation and regulatory compliance solutions to FDA-regulated industry, announced the formation of a new practice group to provide process analytical technology (PAT) services to pharmaceutical manufacturing clients worldwide. PAT is a system for designing, analyzing, and controlling manufacturing through timely measurements of critical quality and performance attributes of raw and in-process materials and processes, with the goal of ensuring final product quality at the end of the manufacturing process. PAT services are a natural extension of Lloyd’s Register Serentec’s existing portfolio of process and automation systems validation consulting services.
