Quality management has been an important focus for IGL. Quality
representatives are dedicated for each of our companies and sites.
- All of the IGL’s activities managed by the QMS have ISO 13485 certification.
- Our products intended to the European market hold the CE mark.
- IGL drugs are manufactured in a Pharmaceutical Establishment GMP certified site.
- Our machines perfusion and our organ solutions are proudly made in
the United States and in France respectively. We firmly believe that
products made in the United States and in France are some of the highest
quality and most durable products in the world.
- Identification and Traceability of our products are ensured by our
fully validated ERP (Enterprise Resource Planning) system that connects
all of IGL companies.
With its careful QMS, IGL is committed to advocating the customer
interest, by enforcing regulatory and legal requirements in order to improve our products, to meet the needs of our customers and earn their trust.