Cmed Group will showcase its full-service CRO capabilities at the DIA‚Äôs Annual Meeting 2013, as well as demonstrate the latest version of Timaeus, its innovative, cloud-based eClinical platform to manage data from Study Design through Reporting.
Online PR News – 05-June-2013 – Horsham, UK – Cmed Group will showcase its full-service CRO capabilities at the DIA‚Äôs Annual Meeting 2013 (June 23-27, 2013, Boston Convention and Exhibition Center, Boston, Massachusetts, USA) as well as demonstrate the latest version of Timaeus, its innovative, cloud-based eClinical platform to manage data from Study Design through Reporting.
Through the coupling of full service trial delivery teams and trusted technology, Cmed Group has a proven track record of helping the biopharmaceutical industry design and deliver both innovative and traditional early phase I to IIb clinical trials, as well as increasingly being asked by clients to take on their phase III projects.
Cmed has seen accelerating demand for strategic advice and drug development consulting, both in terms of study design and CDP development, and therefore has been expanding its in-house Drug Development Consulting, Regulatory & Medical Affairs Group. Visitors to Booth #858 can take advantage of obtaining expert advice on various topics from this highly experienced team, including Geoff Fatzinger, Vice President of Global Medical and Regulatory Affairs. Visitors can also discover how the company‚Äôs skilled Project Managers and geographically based CRAs deliver projects to time, budget and quality, as well as hear about Cmed‚Äôs biometrics solutions for full-service trials or as a stand-alone service.
In addition, visitors will receive personal demonstrations of Cmed‚Äôs impressive e-clinical technology, Timaeus, and learn how study teams can quickly, easily and cost‚Äźeffectively build and manage clinical research studies. Timaeus features new streamlined interfaces with improved query management and source data verification workflow. Investigators and Monitors are able to work from a dynamic to-do list while Monitors quickly access study metrics from a new custom dashboard. Cmed will also highlight how Timaeus Guided Trial Builder enables non-programmers to very rapidly build entire trials, including visit schedules, pages and edit checks. Adding Guided Trial Builder to Timaeus‚Äô on-demand deployment capabilities enables study teams to build validated trials from a global library of standards, eliminating QC and manual hand-off delays during the study start up process.
To find out more about Cmed‚Äôs CRO services and Timaeus, visit Booth #858 at DIA 2013 Annual Meeting at the Boston Convention and Exhibition Center on June 23-27, 2013. Alternatively, visit www.cmedgroup.com for more information.