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X-WR-CALDESC:Events for GKM Gesellschaft für Therapieforschung mbH | Full-service CRO
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BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220330T150000
DTEND;TZID=Europe/Berlin:20220330T160000
DTSTAMP:20260607T120619
CREATED:20220314T133137Z
LAST-MODIFIED:20220314T133137Z
UID:6892-1648652400-1648656000@www.gkm-therapieforschung.de
SUMMARY:Studie läuft\, aber wo bleiben die Patienten?
DESCRIPTION:In German language: \nDeepDive in Online-Patientenrekrutierung \nDie Patientenrekrutierung bei klinischen Studien kann herausfordernd sein. In diesem Webinar diskutieren Dr. Andrea Röthler\, Abteilungsleiterin Projektmanagement der Gesellschaft für Therapieforschung mbH\, und Dr. Tobias Kruse\, CEO Trials24\, über Hürden und Möglichkeiten der dezentralen Patientenrekrutierung\, außerhalb der Prüfzentren. Das praxisnahe Webinar richtet sich an Sponsoren\, die sich über die Online-Patientenrekrutierung informieren wollen und bietet die Chance eines interaktiven Austausches. \nAnmeldung per LinkedIn \nAnmeldung per Anmeldeformular
URL:https://www.gkm-therapieforschung.de/en/event/studie-laeuft-aber-wo-bleiben-die-patienten/
LOCATION:Live demo webinar via Teams
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220406T130000
DTEND;TZID=Europe/Berlin:20220406T173000
DTSTAMP:20260607T120619
CREATED:20220110T175725Z
LAST-MODIFIED:20220110T175725Z
UID:6860-1649250000-1649266200@www.gkm-therapieforschung.de
SUMMARY:clinical requirements
DESCRIPTION:MEGRA\, start-up medical devices and MDR \nAn online course with 8 modules from 1:00 p.m. to 5:30 p.m.\nDr. Andrea Röthler gives a lecture on the subject of clinical requirements. \nModule 5: Clinical Requirements \nWednesday\, April 6th\, 2022 \nSpeakers:\nDr. Raymond Nistor (QMD Services GmbH)\nDr. Andrea Röthler (GKM Society for Therapy Research) \nSubjects: \n\nClinical testing\, classification and categorization\nWhich requirements must clinical data meet for which purpose?\n\nDo you want to know more?\nThen download the entire MEGRA e.V. program here.
URL:https://www.gkm-therapieforschung.de/en/event/clinical-requirements/
LOCATION:Live demo webinar via Teams
CATEGORIES:Online-Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220412T140000
DTEND;TZID=Europe/Berlin:20220412T153000
DTSTAMP:20260607T120619
CREATED:20220103T122803Z
LAST-MODIFIED:20220103T123209Z
UID:6825-1649772000-1649777400@www.gkm-therapieforschung.de
SUMMARY:PharmaFORUM Webcast Medical Affairs
DESCRIPTION:One live webcast per month with proven experts from medical affairs with the possibility of discussion via audio and chat. Practical information in short periods of time at your workplace or on the go. Live broadcast available afterwards. Lecture documents can be downloaded. You participate in your device from different locations. You can see the presentation documents and hear the talk of our speakers. You also have the opportunity to ask questions before and during the webcast\, which our speakers will be happy to answer individually. \nApril 12th\, 2021\, 2 p.m. \nRupert Lang\, Chief Operations Officer GKM\, on application monitoring (study synopsis\, notification\, ethics vote\, etc.)
URL:https://www.gkm-therapieforschung.de/en/event/pharmaforum-webcast-medical-affairs/
LOCATION:Live demo webinar via Teams
CATEGORIES:Online-Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20220501
DTEND;VALUE=DATE:20220502
DTSTAMP:20260607T120619
CREATED:20220104T182547Z
LAST-MODIFIED:20220104T182847Z
UID:6839-1651363200-1651449599@www.gkm-therapieforschung.de
SUMMARY:Clinical trials of medical devices
DESCRIPTION:Medical devices have to be safe and efficient. Appropriate clinical data are required to substantiate this. Dr. Andrea Röthler gives a lecture in an online event on the subject of clinical trials with medical devices: \nPMCF studies\, planned date April / May 2022
URL:https://www.gkm-therapieforschung.de/en/event/clinical-trials-of-medical-devices/
LOCATION:Live demo webinar via Teams
CATEGORIES:Online-Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220720T150000
DTEND;TZID=Europe/Berlin:20220720T160000
DTSTAMP:20260607T120619
CREATED:20220620T092618Z
LAST-MODIFIED:20220621T163910Z
UID:6923-1658329200-1658332800@www.gkm-therapieforschung.de
SUMMARY:Webinar: EU Clinical Trial Regulation 536/2014 (CTR): Was ist bei der Umsetzung zu beachten?
DESCRIPTION:In German language: \nSeit dem 31.01.2022 ist die Clinical Trial Regulation 536/2014 (CTR) in der Praxis anwendbar. Es gibt eine Übergangsfrist von drei Jahren\, in der sowohl die EU Richtlinie 2001/20 als auch die EU Verordnung 536/2014 parallel laufen. Dieses praxisorientierte Webinar richtet sich an Sponsoren\, die sich Klarheit über die wichtigsten Änderungen und Anforderungen im Rahmen der EU CTR sowie der Übergangsphase verschaffen wollen. Zudem bietet es die Chance\, Fragen zu stellen und sich auszutauschen. \nAnmeldung hier: \nhttps://forms.gle/ztAKmpgVACiq36sy9
URL:https://www.gkm-therapieforschung.de/en/event/webinar-eu-clinical-trial-regulation-536-2014-ctr-what-to-consider-during-implementation-in-german/
CATEGORIES:Online-Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20241010T103000
DTEND;TZID=Europe/Berlin:20241010T113000
DTSTAMP:20260607T120619
CREATED:20240805T113833Z
LAST-MODIFIED:20240807T064827Z
UID:8144-1728556200-1728559800@www.gkm-therapieforschung.de
SUMMARY:Webinar Clincase EDC - Bringing precision and efficiency to your clinical studies
DESCRIPTION:  \nWe are pleased to invite you to this webinar to find out about the latest developments in Electronic Data Capture (EDC) systems for clinical research. \nAs a full service CRO offering services throughout the entire clinical development\, we understand the critical role of EDC in ensuring the success of clinical studies and are committed to providing the most efficient and high-quality solutions. With this in mind\, we have organised a webinar together with one of our EDC suppliers\, our longstanding partner Clincase\, for you to find out about the latest developments in EDC systems for clinical research. \nRegister now to learn about new features in Clincase and how you can use them to optimise your clinical trials: \n\nSimplify local lab management for site teams\nUpdating of brand colours and a more modernized interface\nEnable self-configured dashboard with multiple pages in the new reporting and dashboard.\n\nAfter the webinar\, you will have the opportunity to ask our Clincase experts any questions you may have. \nWe look forward to your registration! \nWebinar registration
URL:https://www.gkm-therapieforschung.de/en/event/webinar-clincase-edc-bringing-precision-and-efficiency-to-your-clinical-studies/
LOCATION:Live demo webinar via Teams
CATEGORIES:Online-Seminar
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