DNV GL

MDR Training Course e-learning

Elearning_NuoveISO

A foundation course designed to walk the participants through the key elements and main changes in the Medical Device Regulation EU 2017/745 compared to the Medical Device Directive.

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

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Durata del corso:

8 ore circa

Prezzo:

220 euro + iva

Product Assurance:

MDR training course

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

Modulo e-learning (per iscriverti clicca sul titolo del corso)