Praxis-Workshop: Market authorization of medical devices
Mercure Hotel Stuttgart Airport Messe Eichwiesenring 1/1, Stuttgart, DeutschlandThis practical workshop closes the information gap on the effects of MDR on the approval process of medical devices and accompanies you step-by-step and through practical examples through the entire process of medical device approval.
Find out moreDVMD-Symposium clinical research
Adapted to the ongoing pandemic, the symposium will be held online via zoom. It is dedicated to current topics in clinical research, including big data, ePRO and risk-based monitoring.
Find out morePraxis-Workshop: Market authorization of medical devices
Hotel NH Potsdam Friedrich-Ebert-Straße 88, Potsdam, DeutschlandThis practical workshop closes the information gap on the effects of MDR on the approval process of medical devices and accompanies you step-by-step and through practical examples through the entire process of medical device approval.
Find out more28th BVMA Symposium 2020
Sheraton München, Arabellapark Hotel Arabellastr. 5, MünchenMeet us at the 28th BVMA Symposium in Munich. Topics come soon.
Find out moreKeynote lecture “Successfully mastering PMCF studies in the context of clinical follow-up”
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.
Find out more29th BVMA Symposium 2021
Science Congress Center Munich Walther-von-Dyck-Straße 10, Garching, DeutschlandMeet us at the 29th BVMA Symposium in Garching.
Find out moreStudie läuft, aber wo bleiben die Patienten?
Live demo webinar via TeamsDie 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.
Find out moreclinical requirements
Live demo webinar via TeamsMEGRA, start-up medical devices and MDR. Online course with 8 modules from 1:00 p.m. to 5:30 p.m. Dr. Andrea Röthler gives a lecture on the subject of clinical requirements.
Find out morePharmaFORUM Webcast Medical Affairs
Live demo webinar via TeamsOne live webcast per month with proven experts from medical affairs with the possibility of discussion via audio and chat. Rupert Lang, GKM Gesellschaft für Therapieforschung mbH, Chief Operations Officer, gives a lecture on application monitoring (study synopsis, notification, ethical vote, etc.)
Find out moreClinical trials of medical devices
Live demo webinar via TeamsMedical 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: PMCF studies, planned date April / May 2022
Find out moreWebinar: EU Clinical Trial Regulation 536/2014 (CTR): Was ist bei der Umsetzung zu beachten?
In German language: Seit 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.
Find out moreWebinar Clincase EDC – Bringing precision and efficiency to your clinical studies
Live demo webinar via TeamsAs 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. We look forward to your registration!
Find out more