Aim of the MDR Training Course - e-learning

• Understand the intent of the MDR and its requirements;
• Identify the key changes compared to the MDD;
• Define the scope of the regulation and its impact;
• Learn on the interpretation of the new requirements.

Target of MDR Training Course - e-learning

Auditors, consultants, healthcare professionals, people responsible for regulatory compliance, quality management, clinical evaluation or risk management related to medical devices.

Pre-requisites

Participants must have complete knowledge of the MDD (medical device regulation); the relevant harmonized standards and common specifications; and the MEDDEVs – the guidance documents written by the Competent Authorities.

Language

English