{"id":519,"date":"2023-04-25T10:51:53","date_gmt":"2023-04-25T08:51:53","guid":{"rendered":"https:\/\/ceiso.fr\/en\/?p=519"},"modified":"2023-04-25T10:52:01","modified_gmt":"2023-04-25T08:52:01","slug":"rl12-medical-device-regulation-eu-2017-745-introduction-to-the-regulation","status":"publish","type":"post","link":"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl12-medical-device-regulation-eu-2017-745-introduction-to-the-regulation\/","title":{"rendered":"RL12 – Medical Device Regulation (EU) 2017\/745 – Introduction to the Regulation"},"content":{"rendered":"\n
\n

REF. RL12 – INTRA \/ INTER<\/p>\n\n\n\n

EUROPEAN REGULATIONS<\/p>\n<\/div><\/div>\n\n\n\n

<\/div>\n\n\n\n
\n

COURSE DESCRIPTION<\/h2>\n\n\n\n

The design, production and marketing of Medical Devices in Europe must comply with the requirements of Regulation (EU) 2017\/745.<\/p>\n\n\n\n

Operators in this market must be able to evaluate the impact of these requirements on their products\u2019 compliance, the information to be provided in the technical files and how it is organized so as to define an action plan to ensure compliance.<\/p>\n<\/div><\/div>\n\n\n\n

<\/div>\n\n\n\n
\n\t
\n\t\t

DURATION<\/h3>\n\t\t

1 day \/ 7 hours<\/p>\n\t<\/div>\n\t

\n\t\t\n\t\t

IN-PERSON<\/h3>\n\t<\/div>\n
\n\t\t\n\t\t

VIRTUAL CLASSROOM<\/h3>\n\t<\/div>\n<\/div>\n\n\n\n
\n

OBJECTIVES<\/h2>\n\n\n\n
    \n
  • Understand the regulatory framework for MDs – learn the basics.<\/li>\n\n\n\n
  • Identify the impacts on the products and regulatory documents.<\/li>\n\n\n\n
  • Identify the impacts on the organization (responsibilities, UDI).<\/li>\n\n\n\n
  • Raise the awareness of attendees on the role they play.<\/li>\n<\/ul>\n<\/div><\/div>\n\n\n\n
    <\/div>\n\n\n\n
    \n

    TARGET TRAINEES<\/h2>\n\n\n\n

    Medical Device manufacturers\/subcontractors, and more particularly:\u00a0<\/p>\n\n\n\n

      \n
    • R&D team<\/li>\n\n\n\n
    • Production<\/li>\n\n\n\n
    • Purchasing<\/li>\n\n\n\n
    • Sales<\/li>\n\n\n\n
    • Regulatory Affairs<\/li>\n\n\n\n
    • Quality Management<\/li>\n<\/ul>\n<\/div><\/div>\n\n\n\n
      <\/div>\n\n\n\n
      \n

      PREREQUISITES<\/h2>\n\n\n\n
        \n
      • Familiarity with the Medical Device sector<\/li>\n\n\n\n
      • Familiarity with Regulation (EU) 2017\/745 may facilitate a better understanding of its requirements.<\/li>\n<\/ul>\n<\/div><\/div>\n\n\n\n
        <\/div>\n\n\n\n
        \n

        TRAINING RESOURCES<\/h2>\n\n\n\n
          \n
        • PowerPoint presentation handed out at the end of training<\/li>\n\n\n\n
        • Case studies<\/li>\n\n\n\n
        • Distribution of Regulation (EU) 2017\/745 <\/li>\n\n\n\n
        • Quizzes<\/li>\n<\/ul>\n<\/div><\/div>\n\n\n\n
          <\/div>\n\n\n\n
          \n

          COURSE CONTENT<\/h2>\n\n\n\n

          Participants welcomed and presented\/Course objectives\/Presentation of the course content<\/strong><\/p>\n\n\n\n

            \n
          1. Purpose and scope – definitions<\/li>\n\n\n\n
          2. Economic operators\/Individual responsible for ensuring compliance with the regulation<\/li>\n\n\n\n
          3. Traceability\/identification\/registration of MDs: EUDAMED and UDI<\/li>\n\n\n\n
          4. Classification\/conformity assessment<\/li>\n\n\n\n
          5. General safety and performance requirements<\/li>\n\n\n\n
          6. Clinical data<\/li>\n\n\n\n
          7. Post-market and market surveillance, vigilance<\/li>\n\n\n\n
          8. Technical documentation\n
              \n
            • Technical documentation on the device<\/li>\n\n\n\n
            • Post-market surveillance technical documentation<\/li>\n<\/ul>\n<\/li>\n\n\n\n
            • Roadmap<\/li>\n\n\n\n
            • Summary\/Q&A<\/li>\n\n\n\n
            • Course evaluation and conclusion<\/li>\n<\/ol>\n<\/div><\/div>\n\n\n\n
              <\/div>\n\n\n\n
              \n

              EVALUATION METHODS<\/h2>\n\n\n\n
                \n
              • Course evaluation quiz<\/li>\n\n\n\n
              • Satisfaction survey<\/li>\n\n\n\n
              • Attendance certificate<\/li>\n<\/ul>\n\n\n\n

                This training is assessed based on an evaluation of each individual\u2019s acquisition of knowledge via quizzes during and at the end of the program (success criteria >= 75%).<\/em><\/em><\/p>\n<\/div><\/div>\n","protected":false},"excerpt":{"rendered":"

                REF. RL12 – INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION The design, production and marketing of Medical Devices in Europe must comply with the requirements of Regulation (EU) 2017\/745. Operators in this market must be able to evaluate the impact of these requirements on their products\u2019 compliance, the information to be provided in the technical […]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[19,13],"tags":[],"_links":{"self":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/posts\/519"}],"collection":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/comments?post=519"}],"version-history":[{"count":1,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/posts\/519\/revisions"}],"predecessor-version":[{"id":520,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/posts\/519\/revisions\/520"}],"wp:attachment":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/media?parent=519"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/categories?post=519"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/tags?post=519"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}