We have been adapting our offer to our clients’ needs since 1995.
FOUNDING OF THE COMPANY
In line with the requirements of the Food and Drug Administration (FDA).
FIRST INSPECTION BY THE FDA
American Food and Drug Administration. Issues marketing authorizations for medicinal products in the United States.
COFRAC ACCREDITATION AND ISO 9001 CERTIFICATION
Design certification, analyses, microbiological validation of devices and products, sterilization.
CONSTRUCTION OF PREMISES
2 000 sq. m. of premises including 1,000 sq. m of clean rooms.
(Quality control, medicinal products).
ACQUISITION OF QUALISTÉ
Specializing in engineering, Validation and Metrology.
ACQUISITION OF MEDLAB IN BRAZIL
+ Construction of the 2000 sq. m. clean room extension in Saint-Beauzire.
Change of name : QUALISTÉ becomes Icare Validation.
+ Extension of the premises in Brazil with 500 sq. m. of clean rooms.
Opening of the subsidiary LABORATOIRE ICARE SWITZERLAND.
+ Acquisition of LEMI and PHYCHER BIO DEVELOPPEMENT, companies specializing in biocompatibility.
CREATION OF THE BIOTOX BUSINESS UNIT
(Merger of LEMI and PHYCHER).
Located in Strasbourg, Evreux and Toulouse.
+ Launch of the infrastructure extension project on the Saint-Beauzire site.
To become the leader in regulatory safety for Medical Devices in Europe and South America.