Cmed Presents New Generation Technology to Speed and Streamline Clinical Trials at Dpharm Europe. Graham Belgrave, Chief Operations Officer at Cmed, will introduce encapsia™ in the “Innovative Sources & Solutions: Quickfire Disruptors” session on Wednesday 8 February between 4:30pm and 5:00pm, and highlight how a truly flexible, new seamless approach can simplify and streamline clinical trials.
Throughout the conference, Cmed will demonstrate some of the exciting capabilities of encapsia™ for increasing trial efficiency, improving timelines and reducing cost, at booth #2. encapsia™ is unlike any of the existing "last generation" systems and offers integrated, multiple ways for data capture, including mobile eSource, multi-media capture via an iPad and web eDC via a very modern, fast user interface. Powerful, configurable visualizations give live actionable insights and immediate analytics of a trial, allowing issues and trends to be identified and analyzed easily and rapidly.
Attendees will also be able to find out about Cmed’s full suite of services, which ranges from full-service to stand-alone solutions and functional services, such as biometrics, as well as learn about the company’s significant experience in bringing innovation to the design and conduct of complex and demanding clinical trials.
To schedule a meeting with the Cmed team during Dpharm Europe, contact Louise Holliday, Director of Business Development, at firstname.lastname@example.org.
Cmed is an innovative, full service technology-led CRO. Cmed brings together experienced people and technology, providing customers with a friendly, proactive service, and delivers this service using advanced clinical data capture, management and reporting software and processes. Cmed’s new generation clinical data suite, encapsia™, streamlines the capture, management and reporting of clinical data, saving customers time and money. Clinical data can be captured flexibly by eSource, multi-media and web eDC, while being displayed in live visual insights, providing live analytics, and allowing within suite audit trailed actions. It is fully compliant with regulatory guidelines, and allows integration with existing systems. For more information visit www.cmedresearch.com.