ISPE's Core Members are pharmaceutical professionals who use expert knowledge to create high-quality, cost-effective GMP solutions.
We lead and facilitate the development of next generation process technologies and innovative technical solutions. On matters of regulation, our focus is on those requirements that impact — or will impact — the licensing of facilities, manufacturing processes and operations and the sustainability of the supply chain over the product lifecycle. We have developed relationships with and continue to provide key access to major regulatory agencies at the most senior levels.
Our Purpose: ISPE delivers technical and operational solutions to support our Members across the global pharmaceutical and biopharmaceutical industry in the manufacture of quality medicines for patients.
ISPE aims to offer increasing and unparalleled value for Members, companies and stakeholders globally and across all constituent parts of the industry. The end result will be the continued improvement and transformation of the pharmaceutical manufacturing industry to better ensure the availability of quality medicines to patients around the world.
Our Guides are relied on globally by industry and regulators to define the industry standards for design, construction and operation of pharmaceutical manufacturing facilities. ISPE’s training, conferences and Knowledge Networks give professionals solutions for their needs and connect them with other professionals to share best practices. We know how to design, build, qualify, license, operate and maintain these complex facilities, including those that manufacture active pharmaceutical ingredients, finished dosage forms, delivery systems and packaging. Through ISPE's branded expertise in these areas we have deep technical knowledge that is applied in a practical manner.