MDCG regulatory reporting guidelines
The MDCG regulatory reporting guidelines are an essential part of the EU's regulatory framework for medical devices. By ensuring that manufacturers report on adverse events, corrective actions, and ongoing safety data, the guidelines help to ensure the safety and efficacy of medical devices used by patients in the EU. It is imperative that manufacturers comply with these guidelines to ensure that their devices can continue to be sold in the EU market and to build trust with the public.
