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.
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.