2020 has been a challenging year for all of us, but we are ready to continue to help to create an healthier word!

The new Medical Device Regulation will be applied also to certain groups of products without an intended medical purpose as though they are medical devices.

Technology & Research in pink!

Thanks also to project approved by Regione Emilia-Romagna within the scope of …

As part of a long term commitment to quality, AD MODUM R&D was able to go through the certification process rapidly. We achieved certification for both ISO 9001 and ISO 13485.

MDR transition is officially postponed for 1 year, but never stop to develop new products! 

In 2019 Instron has started a new co-operation with AD Modum R&D, considering this company a key strategic customer in Biomedical market.

The world is experiencing widespread ongoing transmission of respiratory illness caused by the novel new Coronavirus (COVID-19).

We know very well that, evolving consumer expectations, complex health and technology ecosystems, force health care stakeholders to invest in value-based care, innovative devices in compliance with stringent regulations.