In this protected production space, the activity is dedicated to the moulding of articles for the medical, pharmaceutical and parapharmaceutical sector, with processes that comply with the standards of certified medical devices. (EU Regulation 2017/745)
The cleanroom is equipped with 2 Security airloock system for the entrance of the material and dedicated personnel.
The air is filtered, and the environment monitored by pressure and temperature control systems, subjected to periodic checks on the presence of particulate matter and bacteria.
The cleanroom is ISO 8 qualified.
The company is ISO 13495:2016 certified for the production of components for Medical Devices.
