The ASEPTIC GROUP site once again meets the rigorous standards for quality management of medical devices.
This re-certification represents an important step in maintaining the organisation’s long-standing commitment to the quality, safety and regulatory compliance of its products and processes. ISO 13485 sets out rigorous requirements for process control, risk management, traceability and the development of a strong quality culture. The renewal of certification confirms that the Limonest site continues to meet these requirements, while improving its practices through a continuous improvement approach.
This success reflects the commitment of the entire team and paves the way for the pursuit of excellence.



