{"id":5262,"date":"2022-02-24T12:27:25","date_gmt":"2022-02-24T11:27:25","guid":{"rendered":"https:\/\/www.entecerma.it\/?p=5262"},"modified":"2022-02-24T12:27:46","modified_gmt":"2022-02-24T11:27:46","slug":"legacy-devices-training-course-new-dates-available","status":"publish","type":"post","link":"https:\/\/www.entecerma.it\/en\/legacy-devices-training-course-new-dates-available\/","title":{"rendered":"Legacy Devices Training Course: new dates available!"},"content":{"rendered":"\n

Save the date on 22 and 23 March 2022 with the ECM Academy training for manufacturers of medical devices certified according to Directive 93\/42\/EEC, pursuant to Article 120 of the MDR.<\/em><\/strong><\/h2>\n\n

Following the success of the first edition and the great demand from those who couldn’t attend, the Course \u201cLEGACY DEVICES, how to prepare for the MDD\/MDR transition using post-market data in the transitional period\u201d<\/strong> is back.<\/p>\n\n

On Tuesday 22 March<\/strong> in Italian and Wednesday 23 March<\/strong> in English, manufacturers will learn how to apply the requirements of Art. 120 of the MDR to devices that are already MDD certified. Through an integrated study<\/strong> of some of the most relevant guidelines<\/strong> published by the MDCG, participants will acquire useful tools to implement MDR requirements, optimizing resources and ensuring compliance with the requirements.<\/p>\n\n

The theoretical study<\/strong> will then be followed – for those who would like to – by an experimental part<\/strong>, which aims to provide practical ideas for understanding which data must be collected during the transition period and how to do so using post-market tools.<\/p>\n\n

<\/div>\n\n
\n
Download the program<\/a><\/div>\n<\/div>\n\n

The course will be divided into two 4-hour modules <\/strong>\u2013 which can be attended separately by remote<\/strong>, to allow companies to participate on the basis of their needs.<\/p>\n\n

The topics<\/strong> covered include:<\/p>\n\n