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DTSTART;VALUE=DATE:20201123
DTEND;VALUE=DATE:20201124
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SUMMARY:DVMD-Symposium clinical research
DESCRIPTION:Adapted to the ongoing pandemic\, the symposium will be held online via zoom.\nIt is dedicated to current topics in clinical research\, including big data\, ePRO and risk-based monitoring. \nDespite or perhaps because of the online format\, discussions\, question and answer sessions and virtual coffee tables are made possible.\nLet yourself be surprised and look forward to exchanging ideas with colleagues.
URL:https://www.gkm-therapieforschung.de/en/event/dvmd-symposium-clinical-research/
CATEGORIES:Online-Seminar
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20201125
DTEND;VALUE=DATE:20201127
DTSTAMP:20260608T015901
CREATED:20200102T163903Z
LAST-MODIFIED:20200102T164157Z
UID:6494-1606262400-1606435199@www.gkm-therapieforschung.de
SUMMARY:Praxis-Workshop: Market authorization of medical devices
DESCRIPTION:After the adoption of the new Medical Device Regulation (MDR) by the European Parliament\, many manufacturers and distributors of medical devices have already started to adapt their processes. However\, although the implementation period for the MDR ends in 2020\, many companies still need information about the effects of the new MDR and how the approval of medical devices will work in the future. This practical workshop closes this information gap and accompanies you step-by-step and through practical examples through the entire process of approval of medical devices.   \nOn the first day you will learn which regulatory requirements you as a manufacturer or distributor of medical devices have to meet\, how the CE marking process works\, how to obtain a clinical evaluation and what you need to consider after placing the medical device on the market. The role of the certified bodies and authorities is explained as well as the tasks of internal monitoring.   \nThe second day focuses on the implementation of the regulatory requirements in the company. Using the example of a specific medical device\, you will get to know the new processes from start to finish. \n \nHot topics \n\n\n\nInnovations in the current medical device regulation \n\n\nLegal basis \n\n\nThe CE marking process using a concrete example \n\n\nCreation of a technical documentation \n\n\nStructure and processes of a quality management system \n\n\nClinical evaluation process \n\n\n \n\nProgram .pdf download here please >>
URL:https://www.gkm-therapieforschung.de/en/event/praxis-workshop-market-authorization-of-medical-devices-3/
LOCATION:Hotel NH Potsdam\, Friedrich-Ebert-Straße 88\, Potsdam\, 14467\, Deutschland
CATEGORIES:Praxis-Workshop
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DTSTART;VALUE=DATE:20201127
DTEND;VALUE=DATE:20201128
DTSTAMP:20260608T015901
CREATED:20200102T162940Z
LAST-MODIFIED:20200102T164453Z
UID:6492-1606435200-1606521599@www.gkm-therapieforschung.de
SUMMARY:28th BVMA Symposium 2020
DESCRIPTION:Meet us at the 28th BVMA Symposium in Munich. Topics come soon.
URL:https://www.gkm-therapieforschung.de/en/event/28th-bvma-symposium-2020/
LOCATION:Sheraton München\, Arabellapark Hotel\, Arabellastr. 5\, München\, 81925
CATEGORIES:Conference
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