PCT Europe 2017, Amsterdam. In partnership with Synergy CRO, Cyntegrity presents the concept of #RealRBM: Hype or Common Sense. The main topics of the presentation are: The concept of integrity in Risk-based Monitoring Risks perception - differences in risk assessment between a sponsor and a CRO [...]
Interested in holistic implementation of the RBM? Let's talk in London by Clinical Operations Strategy Meeting (EU 2016) on Monday 11th July 2016. See the RBM session plan for the meeting: Interested in scheduling a meeting during the conference or after?[button link="https://cyntegrity.com/contact-info/" color="default" size="" stretch="" type="" shape="" [...]
DIA Europe is more than a traditional meeting. It's a chance to learn, engage, and grow as a healthcare professional alongside thousands of cross-functional collaborative leaders. Our CEO, Dr Artem Andrianov, will share his industry insights and expertise as one of the selected speakers. We hope your busy schedule will allow you to meet with Artem.
PCT Europe is back for 2018, bringing you the latest information from across the clinical trials spectrum and providing you with direct access to the industry’s leading innovators.
Our CEO, Dr Artem Andrianov, will share his industry insights and expertise as one of the selected key note speakers. We hope your busy schedule will allow you to meet with Artem.
Our CEO, Dr Artem Andrianov, will chair the RBM round table session and share his industry insights and expertise as one of the selected industry speakers: Tuesday, October 16, 15:15 - Predictive Analytics in RBM
Conference season has started! Our first stop was the Global RBM Summit 2018 in London. Our CSO Dr Johann Proeve was invited to join the conversation as a speaker on the topic “Pragmatic Centralized Monitoring – How to get there?”. Johann shares his observations with us.
The Society for Clinical Data Management (SCDM) is a non-profit, international organization.
Adverse Event (AE) reporting, identified by the FDA as one of the most important challenges in clinical research, is known to be prone to under and over-reporting. When starting a project and considering the various ways available to capture the adverse event data, it’s important to ask yourself some analytical questions that help you improve AE and SAE capturing and reporting.
Sponsor, Speaker....and Many New Features to Demo With a surge of new technologies and trial models being implemented, the time is now to capitalise on industry expertise to capture the cost and efficiency benefits of risk-based monitoring. Join us in London for CBI’s 3rd annual Global [...]