Following a rigorous inspection by the French National Agency for Medicines and Health Products Safety (ANSM), IRCAD has officially renewed its Good Laboratory Practice (GLP) compliance. Effective December 1st, this certification confirms IRCAD’s adherence to international OECD guidelines for the safety testing of innovative medical devices.
This achievement is the result of two years of cross-functional collaboration and significant investment in cutting-edge laboratory and IT infrastructure. By securing this renewal, IRCAD reinforces its position as a premier global hub for preclinical testing, providing industry partners with the high-standard data required for clinical trials and regulatory submissions.
We extend our congratulations to the multidisciplinary teams whose expertise and dedication made this significant milestone possible.