It examines the most common non-conformities identified by Notified Bodies during audits and assessments, offering practical solutions to prevent and effectively manage them.

From EU regulation (MDR/IVDR) to the specific Italian Guidelines [...]

This white paper summarizes the key contents and highlights from the morning roundtables of MDG 2025 – MedGenerAction which took place in Bologna on October 1st, 2025. MDG is the annual reference summit for professionals operating in the Medical Device sector, presented by Complife Group.

This white paper provides an overview of the basic [...]

This white paper brings together some of the key [...]

This White Paper is a concise and practical guide to [...]