Location: Lisbon, Portugal

Description: Three experts will share with you the requirements for MDR and IVDR implementation and the changes from the former Directives. Training is planned for two days but it is possible to book individual days as needed. Topics covered will include: Notified Body selection, working with contract manufacturers, document control, the Qualified Person, economic operators, software validation, labelling and translations, clinical evaluation and clinical evidence, and data protection.

Contact: +49 1 60 92 37 74 84