ADAX is a high quality and experienced provider of complete set of clinical, regulatory and vigilance support to the manufacturers of Medical Devices.

We follow closely rapid changes in the regulatory setting and advise our clients to maintain constant compliance with all regulatory requirements of the EU. Our operational team understands the regulatory implications, so your clinical study or regulatory submission is in safe, expert hands. We can support you in all activities related to regulatory compliance, including obtaining CE Marking and registration of your device.