With the EU MDR, manufacturers must continuously collect clinical data on the performance and safety of their medical devices even after they have been placed on the market. But how do you master PMCF studies in the context of clinical follow-up? In our second informal “MedTech Connect” exchange, it’s all about the PMCF phase, which is immensely important in post-market surveillance. Learn what PMCF should ideally look like, under what conditions manufacturers need to conduct PMCF studies, and how they can make these types of studies a success by following simple ground rules. Together with the GKM Society for Therapy Research we offer you an exciting impulse lecture as well as a space to bring your experiences and problems and to exchange ideas.<\/p>\n
Dr.<\/b> Andrea <\/b>R\u00f6thler<\/b> (head of project management and head of the section medical devices at GKM Gesellschaft f\u00fcr Therapieforschung) leads the workshop \u201cRegistration of Medical Devices\u201d<\/p>\n
The event will be in German, only.<\/p>","excerpt":"
With the EU MDR, manufacturers must continuously collect clinical data on the performance and safety of their medical devices even after they have been placed on the market. But how do you master PMCF studies in the context of clinical follow-up? In our second informal “MedTech Connect” exchange, it’s all about the PMCF phase, which is immensely important in post-market surveillance. Learn what PMCF should ideally look like, under what conditions manufacturers need to conduct PMCF studies, and how they can make these types of studies a success by following simple ground rules. Together with the GKM Society for Therapy Research we offer you an exciting impulse lecture as well as a space to bring your experiences and problems and to exchange ideas.<\/p>","slug":"keynote-lecture-successfully-mastering-pmcf-studies-in-the-context-of-clinical-follow-up","image":false,"all_day":false,"start_date":"2021-05-20 16:00:00","start_date_details":{"year":"2021","month":"05","day":"20","hour":"16","minutes":"00","seconds":"00"},"end_date":"2021-05-20 17:00:00","end_date_details":{"year":"2021","month":"05","day":"20","hour":"17","minutes":"00","seconds":"00"},"utc_start_date":"2021-05-20 14:00:00","utc_start_date_details":{"year":"2021","month":"05","day":"20","hour":"14","minutes":"00","seconds":"00"},"utc_end_date":"2021-05-20 15:00:00","utc_end_date_details":{"year":"2021","month":"05","day":"20","hour":"15","minutes":"00","seconds":"00"},"timezone":"Europe\/Berlin","timezone_abbr":"CEST","cost":"","cost_details":{"currency_symbol":"","currency_code":"","currency_position":"prefix","values":[]},"website":"https:\/\/discover.climedo.com\/de\/klinische-studien-in-der-post-market-phase","show_map":false,"show_map_link":false,"hide_from_listings":false,"sticky":false,"featured":false,"categories":[],"tags":[],"venue":[],"organizer":[{"id":6675,"author":"56","status":"publish","date":"2021-05-03 14:23:53","date_utc":"2021-05-03 12:23:53","modified":"2021-05-03 14:23:53","modified_utc":"2021-05-03 12:23:53","url":"https:\/\/www.gkm-therapieforschung.de\/organizer\/climedo\/","organizer":"Climedo Health GmbH","slug":"climedo","website":"https:\/\/climedo.de\/","json_ld":{"@type":"Person","name":"Climedo Health GmbH","description":"","url":"https:\/\/climedo.de\/","telephone":"","email":"","sameAs":"https:\/\/climedo.de\/"},"global_id":"www.gkm-therapieforschung.de\/en\/?id=6675","global_id_lineage":["www.gkm-therapieforschung.de\/en\/?id=6675"]}],"custom_fields":[],"json_ld":{"@context":"http:\/\/schema.org","@type":"Event","name":"Keynote lecture “Successfully mastering PMCF studies in the context of clinical follow-up”","description":"<p>With the EU MDR, manufacturers must continuously collect clinical data on the performance and safety of their medical devices even after they have been placed on the market. But how do you master PMCF studies in the context of clinical follow-up? In our second informal "MedTech Connect" exchange, it\\'s all about the PMCF phase, which is immensely important in post-market surveillance. Learn what PMCF should ideally look like, under what conditions manufacturers need to conduct PMCF studies, and how they can make these types of studies a success by following simple ground rules. Together with the GKM Society for Therapy Research we offer you an exciting impulse lecture as well as a space to bring your experiences and problems and to exchange ideas.<\/p>\\n","url":"https:\/\/www.gkm-therapieforschung.de\/en\/event\/keynote-lecture-successfully-mastering-pmcf-studies-in-the-context-of-clinical-follow-up\/","eventAttendanceMode":"https:\/\/schema.org\/OfflineEventAttendanceMode","eventStatus":"https:\/\/schema.org\/EventScheduled","startDate":"2021-05-20T16:00:00+02:00","endDate":"2021-05-20T17:00:00+02:00","organizer":{"@type":"Person","name":"Climedo Health GmbH","description":"","url":"https:\/\/climedo.de\/","telephone":"","email":"","sameAs":"https:\/\/climedo.de\/"},"performer":"Organization"}}