Esteve Química has always been an internationally oriented manufacturing company committed to the high quality standards of pharmaceutical industry.
Our reliability derives from high standards of quality, supply chain management, engineering and maintenance, as well as from accountability and flexible practice.
Our facilities are regularly inspected by Health Authorities (FDA, European Authorities, PMDA...). The continuous implementation and follow-up of cGMPs, added to our fully dedicated Customer Service and Regulatory Affairs teams, allows our global quality system to meet the highest standards of compliance with the flexibility required to adjust to our customers’ needs.
Esteve Química’s Quality System is based on cGMPs as well as on the latest trends.
A global Quality Compliance system implemented worldwide
Esteve Química’s Quality System has been regularly inspected by national authorities, with the first FDA inspection being conducted in 1978 (31 inspections of the agency have been performed since that date).
Esteve Química implements an Environment, Health & Safety (EHS) management model based on the principles of the Esteve Code of Ethics and particularly the Environment, Health and Safety Policy of the Esteve Group.