Suvoda is joining this year's Clinical Operations in Oncology Trials Europe Conference in a major way! We'll be exhibiting, presenting and participating in a panel with industry peers. Our experts will be at booth #9, ready to show you how our precision-built eConsent, IRT and eCOA platform can optimize your oncology trial. Schedule a demo or meeting with one of our team members at the booth.
For more information, please attend one of the following sessions.
Presentation
Tuesday, November 28th | 9:30am
Precision technologies for precision trials: streamlining patients', sites' and sponsors' trial experience
- Specific clinical trials operations challenges created by the uncertainties inherent in oncology trials
- How eConsent, IRT and eCOA can be set up to maximize sponsors' operational efficiency and minimize stress on clinical teams
- Oncology case studies from Suvoda's portfolio to demonstrate how flexible IRT functionalities can help novel trial designs in oncology trials run more smoothly and streamline bringing medications to market
- The implications of future innovations in cancer treatment and how that may impact oncology trials and the technology designed to support them
Speaker: Daniela Duffett, Senior Solutions Consultant
Panel
Tuesday, November 28th | 2:30pm
Analysing key functions to reduce study start-up time and bring your drug to market quicker
- Preparing for possible hurdles which can often slow down trials and in-turn, result increased costs
- Identifying innovative technologies that can assist in the swift startup of a clinical trial
- Sharing experiences in trial design, the do's the don'ts of early stage trials
Chair: Sonnika Lamont, Analyst, GlobalData
Panelists:
Andriy Krendyukov, VP Medical Affairs and Clinical Development /PhD fellow at Mannheim University (Innovation and Management)
Stefano Ferrara, Director of Clinical Science, BeiGene
Jessica Cordes, Clinical Operations Expert
Daniela Duffett, Senior Solutions Consultant, Suvoda
